Canonical Allele Identifier: CA3077272

Gene: MFSD8

Linked Data

• dbSNP Id: rs768627011
• ExAC: 4:128842849 C / A
• gnomAD v2: 4-128842849-C-A
• gnomAD v3: 4-127921694-C-A
• gnomAD v4: 4-127921694-C-A
• MyVariant Identifiers: chr4:g.128842849C>A (hg19) ; chr4:g.127921694C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.127921694C>A , CM000666.2:g.127921694C>A	GRCh38
NC_000004.11:g.128842849C>A , CM000666.1:g.128842849C>A	GRCh37
NC_000004.10:g.129062299C>A	NCBI36
NG_008657.1:g.49291G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296468.8:c.1180G>T	ENSP00000296468.3:p.Asp394Tyr
ENST00000509826.2:c.*501G>T	ENSP00000421176.2:n.*501G>T
ENST00000513559.6:c.898G>T	ENSP00000425000.2:p.Asp300Tyr
ENST00000515130.6:c.*65G>T	ENSP00000493056.1:n.*65G>T
ENST00000641025.1:c.*65G>T	ENSP00000493346.1:n.*65G>T
ENST00000641092.1:c.*65G>T	ENSP00000493392.1:n.*65G>T
ENST00000641133.1:c.*494G>T	ENSP00000493192.1:n.*494G>T
ENST00000641146.1:n.1046G>T
ENST00000641147.1:c.730G>T	ENSP00000493133.1:p.Asp244Tyr
ENST00000641178.1:c.1045G>T	ENSP00000492989.1:p.Asp349Tyr
ENST00000641186.1:c.1066G>T	ENSP00000493347.1:p.Asp356Tyr
ENST00000641228.1:c.*65G>T	ENSP00000493194.1:n.*65G>T
ENST00000641332.1:c.*241G>T	ENSP00000493397.1:n.*241G>T
ENST00000641340.1:c.*309G>T	ENSP00000493191.1:n.*309G>T
ENST00000641388.1:n.427G>T
ENST00000641393.1:c.730G>T	ENSP00000493197.1:p.Asp244Tyr
ENST00000641397.1:c.*65G>T	ENSP00000493406.1:n.*65G>T
ENST00000641413.1:c.105G>T
ENST00000641434.1:c.1180G>T	ENSP00000493279.1:p.Asp394Tyr
ENST00000641464.1:c.*413G>T	ENSP00000493438.1:n.*413G>T
ENST00000641482.1:c.*65G>T	ENSP00000493277.1:n.*65G>T
ENST00000641508.1:c.*413G>T	ENSP00000493209.1:n.*413G>T
ENST00000641509.1:c.865G>T	ENSP00000493459.1:p.Asp289Tyr
ENST00000641590.1:c.*65G>T	ENSP00000493132.1:n.*65G>T
ENST00000641658.1:c.*345G>T	ENSP00000492987.1:n.*345G>T
ENST00000641686.2:c.1180G>T MANE Select	ENSP00000493218.2:p.Asp394Tyr
ENST00000641690.1:c.979G>T	ENSP00000492966.1:p.Asp327Tyr
ENST00000641742.1:c.*345G>T	ENSP00000493315.1:n.*345G>T
ENST00000641748.1:c.1180G>T	ENSP00000493330.1:p.Asp394Tyr
ENST00000641753.1:c.1007G>T
ENST00000641774.1:c.*432G>T	ENSP00000492960.1:n.*432G>T
ENST00000641830.1:c.412G>T
ENST00000641843.1:c.*241G>T	ENSP00000493174.1:n.*241G>T
ENST00000641869.1:c.381G>T
ENST00000641870.1:c.*241G>T	ENSP00000493044.1:n.*241G>T
ENST00000641882.1:c.*345G>T	ENSP00000493301.1:n.*345G>T
ENST00000641928.1:c.*309G>T	ENSP00000493418.1:n.*309G>T
ENST00000641949.1:c.554-858G>T	ENSP00000492891.1:n.554-858G>T
ENST00000642012.1:n.1044G>T
ENST00000642034.1:c.*65G>T	ENSP00000493285.1:n.*65G>T
ENST00000642042.1:c.1180G>T	ENSP00000493260.1:p.Asp394Tyr
ENST00000642078.1:c.*241G>T	ENSP00000492885.1:n.*241G>T
ENST00000296468.7:c.1180G>T	ENSP00000296468.3:p.Asp394Tyr
ENST00000504126.1:n.208G>T
ENST00000513559.5:c.1045G>T	ENSP00000425000.1:p.Asp349Tyr
ENST00000515130.5:n.1522G>T
NM_152778.2:c.1180G>T	NP_689991.1:p.Asp394Tyr
XM_005262893.1:c.1180G>T	XP_005262950.1:p.Asp394Tyr
XM_005262896.1:c.1033G>T	XP_005262953.1:p.Asp345Tyr
XM_005262897.1:c.979G>T	XP_005262954.1:p.Asp327Tyr
XM_005262898.2:c.*65G>T	XP_005262955.1:n.*65G>T
XM_011531830.1:c.1066G>T	XP_011530132.1:p.Asp356Tyr
XM_011531831.1:c.865G>T	XP_011530133.1:p.Asp289Tyr
XM_011531832.1:c.*65G>T	XP_011530134.1:n.*65G>T
XR_938717.1:n.1257G>T
NM_001363520.1:c.979G>T	NP_001350449.1:p.Asp327Tyr
NM_001363521.1:c.865G>T	NP_001350450.1:p.Asp289Tyr
XM_005262898.3:c.*65G>T	XP_005262955.1:n.*65G>T
XM_017007989.1:c.*65G>T	XP_016863478.1:n.*65G>T
XM_024453981.1:c.1045G>T	XP_024309749.1:p.Asp349Tyr
XM_024453982.1:c.931G>T	XP_024309750.1:p.Asp311Tyr
XM_024453983.1:c.730G>T	XP_024309751.1:p.Asp244Tyr
XR_001741194.1:n.1153G>T
XR_001741195.1:n.1039G>T
XR_001741196.1:n.952G>T
XR_001741197.1:n.1112G>T
XR_001741198.2:n.1008G>T
XR_001741199.1:n.1008G>T
XR_938717.2:n.1257G>T
NM_001363520.2:c.979G>T	NP_001350449.1:p.Asp327Tyr
NM_001363521.2:c.865G>T	NP_001350450.1:p.Asp289Tyr
NM_001371590.1:c.1045G>T	NP_001358519.1:p.Asp349Tyr
NM_001371591.1:c.1180G>T	NP_001358520.1:p.Asp394Tyr
NM_001371592.1:c.1186G>T	NP_001358521.1:p.Asp396Tyr
NM_001371593.1:c.1066G>T	NP_001358522.1:p.Asp356Tyr
NM_001371594.1:c.1033G>T	NP_001358523.1:p.Asp345Tyr
NM_001371595.1:c.898G>T	NP_001358524.1:p.Asp300Tyr
NM_001371596.2:c.1180G>T MANE Select	NP_001358525.1:p.Asp394Tyr
NM_152778.3:c.1180G>T	NP_689991.1:p.Asp394Tyr
NM_152778.4:c.1180G>T	NP_689991.1:p.Asp394Tyr