Canonical Allele Identifier: CA441376027

Gene: MFSD8

Linked Data

• MyVariant Identifiers: chr4:g.128842829A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.127921674A>G , CM000666.2:g.127921674A>G	GRCh38
NC_000004.11:g.128842829A>G , CM000666.1:g.128842829A>G	GRCh37
NC_000004.10:g.129062279A>G	NCBI36
NG_008657.1:g.49311T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296468.8:c.1200T>C	ENSP00000296468.3:p.Gly400=
ENST00000509826.2:c.*521T>C	ENSP00000421176.2:n.*521T>C
ENST00000513559.6:c.918T>C	ENSP00000425000.2:p.Gly306=
ENST00000515130.6:c.*85T>C	ENSP00000493056.1:n.*85T>C
ENST00000641025.1:c.*85T>C	ENSP00000493346.1:n.*85T>C
ENST00000641092.1:c.*85T>C	ENSP00000493392.1:n.*85T>C
ENST00000641133.1:c.*514T>C	ENSP00000493192.1:n.*514T>C
ENST00000641146.1:n.1066T>C
ENST00000641147.1:c.750T>C	ENSP00000493133.1:p.Gly250=
ENST00000641178.1:c.1065T>C	ENSP00000492989.1:p.Gly355=
ENST00000641186.1:c.1086T>C	ENSP00000493347.1:p.Gly362=
ENST00000641228.1:c.*85T>C	ENSP00000493194.1:n.*85T>C
ENST00000641332.1:c.*261T>C	ENSP00000493397.1:n.*261T>C
ENST00000641340.1:c.*329T>C	ENSP00000493191.1:n.*329T>C
ENST00000641388.1:n.447T>C
ENST00000641393.1:c.750T>C	ENSP00000493197.1:p.Gly250=
ENST00000641397.1:c.*85T>C	ENSP00000493406.1:n.*85T>C
ENST00000641413.1:c.125T>C
ENST00000641434.1:c.1200T>C	ENSP00000493279.1:p.Gly400=
ENST00000641464.1:c.*433T>C	ENSP00000493438.1:n.*433T>C
ENST00000641482.1:c.*85T>C	ENSP00000493277.1:n.*85T>C
ENST00000641508.1:c.*433T>C	ENSP00000493209.1:n.*433T>C
ENST00000641509.1:c.885T>C	ENSP00000493459.1:p.Gly295=
ENST00000641590.1:c.*85T>C	ENSP00000493132.1:n.*85T>C
ENST00000641658.1:c.*365T>C	ENSP00000492987.1:n.*365T>C
ENST00000641686.2:c.1200T>C MANE Select	ENSP00000493218.2:p.Gly400=
ENST00000641690.1:c.999T>C	ENSP00000492966.1:p.Gly333=
ENST00000641742.1:c.*365T>C	ENSP00000493315.1:n.*365T>C
ENST00000641748.1:c.1200T>C	ENSP00000493330.1:p.Gly400=
ENST00000641753.1:c.1027T>C
ENST00000641774.1:c.*452T>C	ENSP00000492960.1:n.*452T>C
ENST00000641830.1:c.432T>C
ENST00000641843.1:c.*261T>C	ENSP00000493174.1:n.*261T>C
ENST00000641869.1:c.401T>C
ENST00000641870.1:c.*261T>C	ENSP00000493044.1:n.*261T>C
ENST00000641882.1:c.*365T>C	ENSP00000493301.1:n.*365T>C
ENST00000641928.1:c.*329T>C	ENSP00000493418.1:n.*329T>C
ENST00000641949.1:c.554-838T>C	ENSP00000492891.1:n.554-838T>C
ENST00000642012.1:n.1064T>C
ENST00000642034.1:c.*85T>C	ENSP00000493285.1:n.*85T>C
ENST00000642042.1:c.1200T>C	ENSP00000493260.1:p.Gly400=
ENST00000642078.1:c.*261T>C	ENSP00000492885.1:n.*261T>C
ENST00000296468.7:c.1200T>C	ENSP00000296468.3:p.Gly400=
ENST00000504126.1:n.228T>C
ENST00000513559.5:c.1065T>C	ENSP00000425000.1:p.Gly355=
ENST00000515130.5:n.1542T>C
NM_152778.2:c.1200T>C	NP_689991.1:p.Gly400=
XM_005262893.1:c.1200T>C	XP_005262950.1:p.Gly400=
XM_005262896.1:c.1053T>C	XP_005262953.1:p.Gly351=
XM_005262897.1:c.999T>C	XP_005262954.1:p.Gly333=
XM_005262898.2:c.*85T>C	XP_005262955.1:n.*85T>C
XM_011531830.1:c.1086T>C	XP_011530132.1:p.Gly362=
XM_011531831.1:c.885T>C	XP_011530133.1:p.Gly295=
XM_011531832.1:c.*85T>C	XP_011530134.1:n.*85T>C
XR_938717.1:n.1277T>C
NM_001363520.1:c.999T>C	NP_001350449.1:p.Gly333=
NM_001363521.1:c.885T>C	NP_001350450.1:p.Gly295=
XM_005262898.3:c.*85T>C	XP_005262955.1:n.*85T>C
XM_017007989.1:c.*85T>C	XP_016863478.1:n.*85T>C
XM_024453981.1:c.1065T>C	XP_024309749.1:p.Gly355=
XM_024453982.1:c.951T>C	XP_024309750.1:p.Gly317=
XM_024453983.1:c.750T>C	XP_024309751.1:p.Gly250=
XR_001741194.1:n.1173T>C
XR_001741195.1:n.1059T>C
XR_001741196.1:n.972T>C
XR_001741197.1:n.1132T>C
XR_001741198.2:n.1028T>C
XR_001741199.1:n.1028T>C
XR_938717.2:n.1277T>C
NM_001363520.2:c.999T>C	NP_001350449.1:p.Gly333=
NM_001363521.2:c.885T>C	NP_001350450.1:p.Gly295=
NM_001371590.1:c.1065T>C	NP_001358519.1:p.Gly355=
NM_001371591.1:c.1200T>C	NP_001358520.1:p.Gly400=
NM_001371592.1:c.1206T>C	NP_001358521.1:p.Gly402=
NM_001371593.1:c.1086T>C	NP_001358522.1:p.Gly362=
NM_001371594.1:c.1053T>C	NP_001358523.1:p.Gly351=
NM_001371595.1:c.918T>C	NP_001358524.1:p.Gly306=
NM_001371596.2:c.1200T>C MANE Select	NP_001358525.1:p.Gly400=
NM_152778.3:c.1200T>C	NP_689991.1:p.Gly400=
NM_152778.4:c.1200T>C	NP_689991.1:p.Gly400=