Canonical Allele Identifier: CA1492804605
Gene: MFSD8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.127921956C= , CM000666.2:g.127921956C= GRCh38
NC_000004.11:g.128843111C= , CM000666.1:g.128843111C= GRCh37
NC_000004.10:g.129062561C= NCBI36
NG_008657.1:g.49029G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296468.8:c.1006G= ENSP00000296468.3:p.Glu336=
ENST00000509826.2:c.*239G= ENSP00000421176.2:n.*239G=
ENST00000513559.6:c.724G= ENSP00000425000.2:p.Glu242=
ENST00000515130.6:c.864-185G= ENSP00000493056.1:n.864-185G=
ENST00000641025.1:c.999-185G= ENSP00000493346.1:n.999-185G=
ENST00000641092.1:c.798-185G= ENSP00000493392.1:n.798-185G=
ENST00000641133.1:c.*320G= ENSP00000493192.1:n.*320G=
ENST00000641146.1:n.872G=
ENST00000641147.1:c.556G= ENSP00000493133.1:p.Glu186=
ENST00000641178.1:c.871G= ENSP00000492989.1:p.Glu291=
ENST00000641186.1:c.892G= ENSP00000493347.1:p.Glu298=
ENST00000641228.1:c.798-185G= ENSP00000493194.1:n.798-185G=
ENST00000641332.1:c.*164-185G= ENSP00000493397.1:n.*164-185G=
ENST00000641340.1:c.*232-185G= ENSP00000493191.1:n.*232-185G=
ENST00000641388.1:n.350-185G=
ENST00000641393.1:c.556G= ENSP00000493197.1:p.Glu186=
ENST00000641397.1:c.684-185G= ENSP00000493406.1:n.684-185G=
ENST00000641413.1:c.28-185G=
ENST00000641434.1:c.1006G= ENSP00000493279.1:p.Glu336=
ENST00000641464.1:c.*239G= ENSP00000493438.1:n.*239G=
ENST00000641482.1:c.999-185G= ENSP00000493277.1:n.999-185G=
ENST00000641508.1:c.*239G= ENSP00000493209.1:n.*239G=
ENST00000641509.1:c.691G= ENSP00000493459.1:p.Glu231=
ENST00000641538.1:c.717G=
ENST00000641590.1:c.885-185G= ENSP00000493132.1:n.885-185G=
ENST00000641658.1:c.*171G= ENSP00000492987.1:n.*171G=
ENST00000641686.2:c.1006G= MANE Select ENSP00000493218.2:p.Glu336=
ENST00000641690.1:c.805G= ENSP00000492966.1:p.Glu269=
ENST00000641742.1:c.*171G= ENSP00000493315.1:n.*171G=
ENST00000641748.1:c.1006G= ENSP00000493330.1:p.Glu336=
ENST00000641753.1:c.833G=
ENST00000641774.1:c.*258G= ENSP00000492960.1:n.*258G=
ENST00000641830.1:c.335-185G=
ENST00000641843.1:c.*164-185G= ENSP00000493174.1:n.*164-185G=
ENST00000641869.1:c.304-185G=
ENST00000641870.1:c.*164-185G= ENSP00000493044.1:n.*164-185G=
ENST00000641882.1:c.*171G= ENSP00000493301.1:n.*171G=
ENST00000641928.1:c.*232-185G= ENSP00000493418.1:n.*232-185G=
ENST00000641949.1:c.554-1120G= ENSP00000492891.1:n.554-1120G=
ENST00000642012.1:n.870G=
ENST00000642034.1:c.885-185G= ENSP00000493285.1:n.885-185G=
ENST00000642042.1:c.1006G= ENSP00000493260.1:p.Glu336=
ENST00000642078.1:c.*164-185G= ENSP00000492885.1:n.*164-185G=
ENST00000296468.7:c.1006G= ENSP00000296468.3:p.Glu336=
ENST00000504126.1:n.34G=
ENST00000505284.5:n.894-185G=
ENST00000509826.1:c.*239G= ENSP00000421176.1:n.*239G=
ENST00000513559.5:c.871G= ENSP00000425000.1:p.Glu291=
ENST00000515130.5:n.1445-185G=
NM_152778.2:c.1006G= NP_689991.1:p.Glu336=
XM_005262893.1:c.1006G= XP_005262950.1:p.Glu336=
XM_005262896.1:c.859G= XP_005262953.1:p.Glu287=
XM_005262897.1:c.805G= XP_005262954.1:p.Glu269=
XM_005262898.2:c.999-185G= XP_005262955.1:n.999-185G=
XM_011531830.1:c.892G= XP_011530132.1:p.Glu298=
XM_011531831.1:c.691G= XP_011530133.1:p.Glu231=
XM_011531832.1:c.885-185G= XP_011530134.1:n.885-185G=
XR_938717.1:n.1083G=
NM_001363520.1:c.805G= NP_001350449.1:p.Glu269=
NM_001363521.1:c.691G= NP_001350450.1:p.Glu231=
XM_005262898.3:c.999-185G= XP_005262955.1:n.999-185G=
XM_017007989.1:c.798-185G= XP_016863478.1:n.798-185G=
XM_024453981.1:c.871G= XP_024309749.1:p.Glu291=
XM_024453982.1:c.757G= XP_024309750.1:p.Glu253=
XM_024453983.1:c.556G= XP_024309751.1:p.Glu186=
XR_001741194.1:n.1076-185G=
XR_001741195.1:n.962-185G=
XR_001741196.1:n.875-185G=
XR_001741197.1:n.938G=
XR_001741198.2:n.931-185G=
XR_001741199.1:n.931-185G=
XR_938717.2:n.1083G=
NM_001363520.2:c.805G= NP_001350449.1:p.Glu269=
NM_001363521.2:c.691G= NP_001350450.1:p.Glu231=
NM_001371590.1:c.871G= NP_001358519.1:p.Glu291=
NM_001371591.1:c.1006G= NP_001358520.1:p.Glu336=
NM_001371592.1:c.1012G= NP_001358521.1:p.Glu338=
NM_001371593.1:c.892G= NP_001358522.1:p.Glu298=
NM_001371594.1:c.859G= NP_001358523.1:p.Glu287=
NM_001371595.1:c.724G= NP_001358524.1:p.Glu242=
NM_001371596.2:c.1006G= MANE Select NP_001358525.1:p.Glu336=
NM_152778.3:c.1006G= NP_689991.1:p.Glu336=
NM_152778.4:c.1006G= NP_689991.1:p.Glu336=