Canonical Allele Identifier: CA441376153

Gene: MFSD8

Linked Data

• MyVariant Identifiers: chr4:g.128842924A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.127921769A>G , CM000666.2:g.127921769A>G	GRCh38
NC_000004.11:g.128842924A>G , CM000666.1:g.128842924A>G	GRCh37
NC_000004.10:g.129062374A>G	NCBI36
NG_008657.1:g.49216T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296468.8:c.1105T>C	ENSP00000296468.3:p.Leu369=
ENST00000509826.2:c.*426T>C	ENSP00000421176.2:n.*426T>C
ENST00000513559.6:c.823T>C	ENSP00000425000.2:p.Leu275=
ENST00000515130.6:c.866T>C	ENSP00000493056.1:p.Phe289Ser
ENST00000641025.1:c.1001T>C	ENSP00000493346.1:p.Phe334Ser
ENST00000641092.1:c.800T>C	ENSP00000493392.1:p.Phe267Ser
ENST00000641133.1:c.*419T>C	ENSP00000493192.1:n.*419T>C
ENST00000641146.1:n.971T>C
ENST00000641147.1:c.655T>C	ENSP00000493133.1:p.Leu219=
ENST00000641178.1:c.970T>C	ENSP00000492989.1:p.Leu324=
ENST00000641186.1:c.991T>C	ENSP00000493347.1:p.Leu331=
ENST00000641228.1:c.800T>C	ENSP00000493194.1:p.Phe267Ser
ENST00000641332.1:c.*166T>C	ENSP00000493397.1:n.*166T>C
ENST00000641340.1:c.*234T>C	ENSP00000493191.1:n.*234T>C
ENST00000641388.1:n.352T>C
ENST00000641393.1:c.655T>C	ENSP00000493197.1:p.Leu219=
ENST00000641397.1:c.686T>C	ENSP00000493406.1:p.Phe229Ser
ENST00000641413.1:c.30T>C
ENST00000641434.1:c.1105T>C	ENSP00000493279.1:p.Leu369=
ENST00000641464.1:c.*338T>C	ENSP00000493438.1:n.*338T>C
ENST00000641482.1:c.1001T>C	ENSP00000493277.1:p.Phe334Ser
ENST00000641508.1:c.*338T>C	ENSP00000493209.1:n.*338T>C
ENST00000641509.1:c.790T>C	ENSP00000493459.1:p.Leu264=
ENST00000641590.1:c.887T>C	ENSP00000493132.1:p.Phe296Ser
ENST00000641658.1:c.*270T>C	ENSP00000492987.1:n.*270T>C
ENST00000641686.2:c.1105T>C MANE Select	ENSP00000493218.2:p.Leu369=
ENST00000641690.1:c.904T>C	ENSP00000492966.1:p.Leu302=
ENST00000641742.1:c.*270T>C	ENSP00000493315.1:n.*270T>C
ENST00000641748.1:c.1105T>C	ENSP00000493330.1:p.Leu369=
ENST00000641753.1:c.932T>C
ENST00000641774.1:c.*357T>C	ENSP00000492960.1:n.*357T>C
ENST00000641830.1:c.337T>C
ENST00000641843.1:c.*166T>C	ENSP00000493174.1:n.*166T>C
ENST00000641869.1:c.306T>C
ENST00000641870.1:c.*166T>C	ENSP00000493044.1:n.*166T>C
ENST00000641882.1:c.*270T>C	ENSP00000493301.1:n.*270T>C
ENST00000641928.1:c.*234T>C	ENSP00000493418.1:n.*234T>C
ENST00000641949.1:c.554-933T>C	ENSP00000492891.1:n.554-933T>C
ENST00000642012.1:n.969T>C
ENST00000642034.1:c.887T>C	ENSP00000493285.1:p.Phe296Ser
ENST00000642042.1:c.1105T>C	ENSP00000493260.1:p.Leu369=
ENST00000642078.1:c.*166T>C	ENSP00000492885.1:n.*166T>C
ENST00000296468.7:c.1105T>C	ENSP00000296468.3:p.Leu369=
ENST00000504126.1:n.133T>C
ENST00000505284.5:n.896T>C
ENST00000513559.5:c.970T>C	ENSP00000425000.1:p.Leu324=
ENST00000515130.5:n.1447T>C
NM_152778.2:c.1105T>C	NP_689991.1:p.Leu369=
XM_005262893.1:c.1105T>C	XP_005262950.1:p.Leu369=
XM_005262896.1:c.958T>C	XP_005262953.1:p.Leu320=
XM_005262897.1:c.904T>C	XP_005262954.1:p.Leu302=
XM_005262898.2:c.1001T>C	XP_005262955.1:p.Phe334Ser
XM_011531830.1:c.991T>C	XP_011530132.1:p.Leu331=
XM_011531831.1:c.790T>C	XP_011530133.1:p.Leu264=
XM_011531832.1:c.887T>C	XP_011530134.1:p.Phe296Ser
XR_938717.1:n.1182T>C
NM_001363520.1:c.904T>C	NP_001350449.1:p.Leu302=
NM_001363521.1:c.790T>C	NP_001350450.1:p.Leu264=
XM_005262898.3:c.1001T>C	XP_005262955.1:p.Phe334Ser
XM_017007989.1:c.800T>C	XP_016863478.1:p.Phe267Ser
XM_024453981.1:c.970T>C	XP_024309749.1:p.Leu324=
XM_024453982.1:c.856T>C	XP_024309750.1:p.Leu286=
XM_024453983.1:c.655T>C	XP_024309751.1:p.Leu219=
XR_001741194.1:n.1078T>C
XR_001741195.1:n.964T>C
XR_001741196.1:n.877T>C
XR_001741197.1:n.1037T>C
XR_001741198.2:n.933T>C
XR_001741199.1:n.933T>C
XR_938717.2:n.1182T>C
NM_001363520.2:c.904T>C	NP_001350449.1:p.Leu302=
NM_001363521.2:c.790T>C	NP_001350450.1:p.Leu264=
NM_001371590.1:c.970T>C	NP_001358519.1:p.Leu324=
NM_001371591.1:c.1105T>C	NP_001358520.1:p.Leu369=
NM_001371592.1:c.1111T>C	NP_001358521.1:p.Leu371=
NM_001371593.1:c.991T>C	NP_001358522.1:p.Leu331=
NM_001371594.1:c.958T>C	NP_001358523.1:p.Leu320=
NM_001371595.1:c.823T>C	NP_001358524.1:p.Leu275=
NM_001371596.2:c.1105T>C MANE Select	NP_001358525.1:p.Leu369=
NM_152778.3:c.1105T>C	NP_689991.1:p.Leu369=
NM_152778.4:c.1105T>C	NP_689991.1:p.Leu369=