Canonical Allele Identifier: CA2672041872
Gene: MFSD8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.127921925dup , CM000666.2:g.127921925dup GRCh38
NC_000004.11:g.128843080dup , CM000666.1:g.128843080dup GRCh37
NC_000004.10:g.129062530dup NCBI36
NG_008657.1:g.49061dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000296468.8:c.1038dup ENSP00000296468.3:p.Val347CysfsTer26
ENST00000509826.2:c.*271dup ENSP00000421176.2:n.*271dup
ENST00000513559.6:c.756dup ENSP00000425000.2:p.Val253CysfsTer26
ENST00000515130.6:c.864-153dup ENSP00000493056.1:n.864-153dup
ENST00000641025.1:c.999-153dup ENSP00000493346.1:n.999-153dup
ENST00000641092.1:c.798-153dup ENSP00000493392.1:n.798-153dup
ENST00000641133.1:c.*352dup ENSP00000493192.1:n.*352dup
ENST00000641146.1:n.904dup
ENST00000641147.1:c.588dup ENSP00000493133.1:p.Val197CysfsTer26
ENST00000641178.1:c.903dup ENSP00000492989.1:p.Val302CysfsTer26
ENST00000641186.1:c.924dup ENSP00000493347.1:p.Val309CysfsTer26
ENST00000641228.1:c.798-153dup ENSP00000493194.1:n.798-153dup
ENST00000641332.1:c.*164-153dup ENSP00000493397.1:n.*164-153dup
ENST00000641340.1:c.*232-153dup ENSP00000493191.1:n.*232-153dup
ENST00000641388.1:n.350-153dup
ENST00000641393.1:c.588dup ENSP00000493197.1:p.Val197CysfsTer26
ENST00000641397.1:c.684-153dup ENSP00000493406.1:n.684-153dup
ENST00000641413.1:c.28-153dup
ENST00000641434.1:c.1038dup ENSP00000493279.1:p.Val347CysfsTer26
ENST00000641464.1:c.*271dup ENSP00000493438.1:n.*271dup
ENST00000641482.1:c.999-153dup ENSP00000493277.1:n.999-153dup
ENST00000641508.1:c.*271dup ENSP00000493209.1:n.*271dup
ENST00000641509.1:c.723dup ENSP00000493459.1:p.Val242CysfsTer26
ENST00000641590.1:c.885-153dup ENSP00000493132.1:n.885-153dup
ENST00000641658.1:c.*203dup ENSP00000492987.1:n.*203dup
ENST00000641686.2:c.1038dup MANE Select ENSP00000493218.2:p.Val347CysfsTer26
ENST00000641690.1:c.837dup ENSP00000492966.1:p.Val280CysfsTer26
ENST00000641742.1:c.*203dup ENSP00000493315.1:n.*203dup
ENST00000641748.1:c.1038dup ENSP00000493330.1:p.Val347CysfsTer26
ENST00000641753.1:c.865dup
ENST00000641774.1:c.*290dup ENSP00000492960.1:n.*290dup
ENST00000641830.1:c.335-153dup
ENST00000641843.1:c.*164-153dup ENSP00000493174.1:n.*164-153dup
ENST00000641869.1:c.304-153dup
ENST00000641870.1:c.*164-153dup ENSP00000493044.1:n.*164-153dup
ENST00000641882.1:c.*203dup ENSP00000493301.1:n.*203dup
ENST00000641928.1:c.*232-153dup ENSP00000493418.1:n.*232-153dup
ENST00000641949.1:c.554-1088dup ENSP00000492891.1:n.554-1088dup
ENST00000642012.1:n.902dup
ENST00000642034.1:c.885-153dup ENSP00000493285.1:n.885-153dup
ENST00000642042.1:c.1038dup ENSP00000493260.1:p.Val347CysfsTer26
ENST00000642078.1:c.*164-153dup ENSP00000492885.1:n.*164-153dup
ENST00000296468.7:c.1038dup ENSP00000296468.3:p.Val347CysfsTer26
ENST00000504126.1:n.66dup
ENST00000505284.5:n.894-153dup
ENST00000509826.1:c.*271dup ENSP00000421176.1:n.*271dup
ENST00000513559.5:c.903dup ENSP00000425000.1:p.Val302CysfsTer26
ENST00000515130.5:n.1445-153dup
NM_152778.2:c.1038dup NP_689991.1:p.Val347CysfsTer26
XM_005262893.1:c.1038dup XP_005262950.1:p.Val347CysfsTer26
XM_005262896.1:c.891dup XP_005262953.1:p.Val298CysfsTer26
XM_005262897.1:c.837dup XP_005262954.1:p.Val280CysfsTer26
XM_005262898.2:c.999-153dup XP_005262955.1:n.999-153dup
XM_011531830.1:c.924dup XP_011530132.1:p.Val309CysfsTer26
XM_011531831.1:c.723dup XP_011530133.1:p.Val242CysfsTer26
XM_011531832.1:c.885-153dup XP_011530134.1:n.885-153dup
XR_938717.1:n.1115dup
NM_001363520.1:c.837dup NP_001350449.1:p.Val280CysfsTer26
NM_001363521.1:c.723dup NP_001350450.1:p.Val242CysfsTer26
XM_005262898.3:c.999-153dup XP_005262955.1:n.999-153dup
XM_017007989.1:c.798-153dup XP_016863478.1:n.798-153dup
XM_024453981.1:c.903dup XP_024309749.1:p.Val302CysfsTer26
XM_024453982.1:c.789dup XP_024309750.1:p.Val264CysfsTer26
XM_024453983.1:c.588dup XP_024309751.1:p.Val197CysfsTer26
XR_001741194.1:n.1076-153dup
XR_001741195.1:n.962-153dup
XR_001741196.1:n.875-153dup
XR_001741197.1:n.970dup
XR_001741198.2:n.931-153dup
XR_001741199.1:n.931-153dup
XR_938717.2:n.1115dup
NM_001363520.2:c.837dup NP_001350449.1:p.Val280CysfsTer26
NM_001363521.2:c.723dup NP_001350450.1:p.Val242CysfsTer26
NM_001371590.1:c.903dup NP_001358519.1:p.Val302CysfsTer26
NM_001371591.1:c.1038dup NP_001358520.1:p.Val347CysfsTer26
NM_001371592.1:c.1044dup NP_001358521.1:p.Val349CysfsTer26
NM_001371593.1:c.924dup NP_001358522.1:p.Val309CysfsTer26
NM_001371594.1:c.891dup NP_001358523.1:p.Val298CysfsTer26
NM_001371595.1:c.756dup NP_001358524.1:p.Val253CysfsTer26
NM_001371596.2:c.1038dup MANE Select NP_001358525.1:p.Val347CysfsTer26
NM_152778.3:c.1038dup NP_689991.1:p.Val347CysfsTer26
NM_152778.4:c.1038dup NP_689991.1:p.Val347CysfsTer26