Canonical Allele Identifier: CA358171296

Gene: MFSD8

Linked Data

• MyVariant Identifiers: chr4:g.128842839C>G (hg19) ; chr4:g.127921684C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.127921684C>G , CM000666.2:g.127921684C>G	GRCh38
NC_000004.11:g.128842839C>G , CM000666.1:g.128842839C>G	GRCh37
NC_000004.10:g.129062289C>G	NCBI36
NG_008657.1:g.49301G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296468.8:c.1190G>C	ENSP00000296468.3:p.Arg397Thr
ENST00000509826.2:c.*511G>C	ENSP00000421176.2:n.*511G>C
ENST00000513559.6:c.908G>C	ENSP00000425000.2:p.Arg303Thr
ENST00000515130.6:c.*75G>C	ENSP00000493056.1:n.*75G>C
ENST00000641025.1:c.*75G>C	ENSP00000493346.1:n.*75G>C
ENST00000641092.1:c.*75G>C	ENSP00000493392.1:n.*75G>C
ENST00000641133.1:c.*504G>C	ENSP00000493192.1:n.*504G>C
ENST00000641146.1:n.1056G>C
ENST00000641147.1:c.740G>C	ENSP00000493133.1:p.Arg247Thr
ENST00000641178.1:c.1055G>C	ENSP00000492989.1:p.Arg352Thr
ENST00000641186.1:c.1076G>C	ENSP00000493347.1:p.Arg359Thr
ENST00000641228.1:c.*75G>C	ENSP00000493194.1:n.*75G>C
ENST00000641332.1:c.*251G>C	ENSP00000493397.1:n.*251G>C
ENST00000641340.1:c.*319G>C	ENSP00000493191.1:n.*319G>C
ENST00000641388.1:n.437G>C
ENST00000641393.1:c.740G>C	ENSP00000493197.1:p.Arg247Thr
ENST00000641397.1:c.*75G>C	ENSP00000493406.1:n.*75G>C
ENST00000641413.1:c.115G>C
ENST00000641434.1:c.1190G>C	ENSP00000493279.1:p.Arg397Thr
ENST00000641464.1:c.*423G>C	ENSP00000493438.1:n.*423G>C
ENST00000641482.1:c.*75G>C	ENSP00000493277.1:n.*75G>C
ENST00000641508.1:c.*423G>C	ENSP00000493209.1:n.*423G>C
ENST00000641509.1:c.875G>C	ENSP00000493459.1:p.Arg292Thr
ENST00000641590.1:c.*75G>C	ENSP00000493132.1:n.*75G>C
ENST00000641658.1:c.*355G>C	ENSP00000492987.1:n.*355G>C
ENST00000641686.2:c.1190G>C MANE Select	ENSP00000493218.2:p.Arg397Thr
ENST00000641690.1:c.989G>C	ENSP00000492966.1:p.Arg330Thr
ENST00000641742.1:c.*355G>C	ENSP00000493315.1:n.*355G>C
ENST00000641748.1:c.1190G>C	ENSP00000493330.1:p.Arg397Thr
ENST00000641753.1:c.1017G>C
ENST00000641774.1:c.*442G>C	ENSP00000492960.1:n.*442G>C
ENST00000641830.1:c.422G>C
ENST00000641843.1:c.*251G>C	ENSP00000493174.1:n.*251G>C
ENST00000641869.1:c.391G>C
ENST00000641870.1:c.*251G>C	ENSP00000493044.1:n.*251G>C
ENST00000641882.1:c.*355G>C	ENSP00000493301.1:n.*355G>C
ENST00000641928.1:c.*319G>C	ENSP00000493418.1:n.*319G>C
ENST00000641949.1:c.554-848G>C	ENSP00000492891.1:n.554-848G>C
ENST00000642012.1:n.1054G>C
ENST00000642034.1:c.*75G>C	ENSP00000493285.1:n.*75G>C
ENST00000642042.1:c.1190G>C	ENSP00000493260.1:p.Arg397Thr
ENST00000642078.1:c.*251G>C	ENSP00000492885.1:n.*251G>C
ENST00000296468.7:c.1190G>C	ENSP00000296468.3:p.Arg397Thr
ENST00000504126.1:n.218G>C
ENST00000513559.5:c.1055G>C	ENSP00000425000.1:p.Arg352Thr
ENST00000515130.5:n.1532G>C
NM_152778.2:c.1190G>C	NP_689991.1:p.Arg397Thr
XM_005262893.1:c.1190G>C	XP_005262950.1:p.Arg397Thr
XM_005262896.1:c.1043G>C	XP_005262953.1:p.Arg348Thr
XM_005262897.1:c.989G>C	XP_005262954.1:p.Arg330Thr
XM_005262898.2:c.*75G>C	XP_005262955.1:n.*75G>C
XM_011531830.1:c.1076G>C	XP_011530132.1:p.Arg359Thr
XM_011531831.1:c.875G>C	XP_011530133.1:p.Arg292Thr
XM_011531832.1:c.*75G>C	XP_011530134.1:n.*75G>C
XR_938717.1:n.1267G>C
NM_001363520.1:c.989G>C	NP_001350449.1:p.Arg330Thr
NM_001363521.1:c.875G>C	NP_001350450.1:p.Arg292Thr
XM_005262898.3:c.*75G>C	XP_005262955.1:n.*75G>C
XM_017007989.1:c.*75G>C	XP_016863478.1:n.*75G>C
XM_024453981.1:c.1055G>C	XP_024309749.1:p.Arg352Thr
XM_024453982.1:c.941G>C	XP_024309750.1:p.Arg314Thr
XM_024453983.1:c.740G>C	XP_024309751.1:p.Arg247Thr
XR_001741194.1:n.1163G>C
XR_001741195.1:n.1049G>C
XR_001741196.1:n.962G>C
XR_001741197.1:n.1122G>C
XR_001741198.2:n.1018G>C
XR_001741199.1:n.1018G>C
XR_938717.2:n.1267G>C
NM_001363520.2:c.989G>C	NP_001350449.1:p.Arg330Thr
NM_001363521.2:c.875G>C	NP_001350450.1:p.Arg292Thr
NM_001371590.1:c.1055G>C	NP_001358519.1:p.Arg352Thr
NM_001371591.1:c.1190G>C	NP_001358520.1:p.Arg397Thr
NM_001371592.1:c.1196G>C	NP_001358521.1:p.Arg399Thr
NM_001371593.1:c.1076G>C	NP_001358522.1:p.Arg359Thr
NM_001371594.1:c.1043G>C	NP_001358523.1:p.Arg348Thr
NM_001371595.1:c.908G>C	NP_001358524.1:p.Arg303Thr
NM_001371596.2:c.1190G>C MANE Select	NP_001358525.1:p.Arg397Thr
NM_152778.3:c.1190G>C	NP_689991.1:p.Arg397Thr
NM_152778.4:c.1190G>C	NP_689991.1:p.Arg397Thr