Canonical Allele Identifier: CA441376093

Gene: MFSD8

Linked Data

• MyVariant Identifiers: chr4:g.128842886T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.127921731T>C , CM000666.2:g.127921731T>C	GRCh38
NC_000004.11:g.128842886T>C , CM000666.1:g.128842886T>C	GRCh37
NC_000004.10:g.129062336T>C	NCBI36
NG_008657.1:g.49254A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296468.8:c.1143A>G	ENSP00000296468.3:p.Glu381=
ENST00000509826.2:c.*464A>G	ENSP00000421176.2:n.*464A>G
ENST00000513559.6:c.861A>G	ENSP00000425000.2:p.Glu287=
ENST00000515130.6:c.*28A>G	ENSP00000493056.1:n.*28A>G
ENST00000641025.1:c.*28A>G	ENSP00000493346.1:n.*28A>G
ENST00000641092.1:c.*28A>G	ENSP00000493392.1:n.*28A>G
ENST00000641133.1:c.*457A>G	ENSP00000493192.1:n.*457A>G
ENST00000641146.1:n.1009A>G
ENST00000641147.1:c.693A>G	ENSP00000493133.1:p.Glu231=
ENST00000641178.1:c.1008A>G	ENSP00000492989.1:p.Glu336=
ENST00000641186.1:c.1029A>G	ENSP00000493347.1:p.Glu343=
ENST00000641228.1:c.*28A>G	ENSP00000493194.1:n.*28A>G
ENST00000641332.1:c.*204A>G	ENSP00000493397.1:n.*204A>G
ENST00000641340.1:c.*272A>G	ENSP00000493191.1:n.*272A>G
ENST00000641388.1:n.390A>G
ENST00000641393.1:c.693A>G	ENSP00000493197.1:p.Glu231=
ENST00000641397.1:c.*28A>G	ENSP00000493406.1:n.*28A>G
ENST00000641413.1:c.68A>G
ENST00000641434.1:c.1143A>G	ENSP00000493279.1:p.Glu381=
ENST00000641464.1:c.*376A>G	ENSP00000493438.1:n.*376A>G
ENST00000641482.1:c.*28A>G	ENSP00000493277.1:n.*28A>G
ENST00000641508.1:c.*376A>G	ENSP00000493209.1:n.*376A>G
ENST00000641509.1:c.828A>G	ENSP00000493459.1:p.Glu276=
ENST00000641590.1:c.*28A>G	ENSP00000493132.1:n.*28A>G
ENST00000641658.1:c.*308A>G	ENSP00000492987.1:n.*308A>G
ENST00000641686.2:c.1143A>G MANE Select	ENSP00000493218.2:p.Glu381=
ENST00000641690.1:c.942A>G	ENSP00000492966.1:p.Glu314=
ENST00000641742.1:c.*308A>G	ENSP00000493315.1:n.*308A>G
ENST00000641748.1:c.1143A>G	ENSP00000493330.1:p.Glu381=
ENST00000641753.1:c.970A>G
ENST00000641774.1:c.*395A>G	ENSP00000492960.1:n.*395A>G
ENST00000641830.1:c.375A>G
ENST00000641843.1:c.*204A>G	ENSP00000493174.1:n.*204A>G
ENST00000641869.1:c.344A>G
ENST00000641870.1:c.*204A>G	ENSP00000493044.1:n.*204A>G
ENST00000641882.1:c.*308A>G	ENSP00000493301.1:n.*308A>G
ENST00000641928.1:c.*272A>G	ENSP00000493418.1:n.*272A>G
ENST00000641949.1:c.554-895A>G	ENSP00000492891.1:n.554-895A>G
ENST00000642012.1:n.1007A>G
ENST00000642034.1:c.*28A>G	ENSP00000493285.1:n.*28A>G
ENST00000642042.1:c.1143A>G	ENSP00000493260.1:p.Glu381=
ENST00000642078.1:c.*204A>G	ENSP00000492885.1:n.*204A>G
ENST00000296468.7:c.1143A>G	ENSP00000296468.3:p.Glu381=
ENST00000504126.1:n.171A>G
ENST00000505284.5:n.934A>G
ENST00000513559.5:c.1008A>G	ENSP00000425000.1:p.Glu336=
ENST00000515130.5:n.1485A>G
NM_152778.2:c.1143A>G	NP_689991.1:p.Glu381=
XM_005262893.1:c.1143A>G	XP_005262950.1:p.Glu381=
XM_005262896.1:c.996A>G	XP_005262953.1:p.Glu332=
XM_005262897.1:c.942A>G	XP_005262954.1:p.Glu314=
XM_005262898.2:c.*28A>G	XP_005262955.1:n.*28A>G
XM_011531830.1:c.1029A>G	XP_011530132.1:p.Glu343=
XM_011531831.1:c.828A>G	XP_011530133.1:p.Glu276=
XM_011531832.1:c.*28A>G	XP_011530134.1:n.*28A>G
XR_938717.1:n.1220A>G
NM_001363520.1:c.942A>G	NP_001350449.1:p.Glu314=
NM_001363521.1:c.828A>G	NP_001350450.1:p.Glu276=
XM_005262898.3:c.*28A>G	XP_005262955.1:n.*28A>G
XM_017007989.1:c.*28A>G	XP_016863478.1:n.*28A>G
XM_024453981.1:c.1008A>G	XP_024309749.1:p.Glu336=
XM_024453982.1:c.894A>G	XP_024309750.1:p.Glu298=
XM_024453983.1:c.693A>G	XP_024309751.1:p.Glu231=
XR_001741194.1:n.1116A>G
XR_001741195.1:n.1002A>G
XR_001741196.1:n.915A>G
XR_001741197.1:n.1075A>G
XR_001741198.2:n.971A>G
XR_001741199.1:n.971A>G
XR_938717.2:n.1220A>G
NM_001363520.2:c.942A>G	NP_001350449.1:p.Glu314=
NM_001363521.2:c.828A>G	NP_001350450.1:p.Glu276=
NM_001371590.1:c.1008A>G	NP_001358519.1:p.Glu336=
NM_001371591.1:c.1143A>G	NP_001358520.1:p.Glu381=
NM_001371592.1:c.1149A>G	NP_001358521.1:p.Glu383=
NM_001371593.1:c.1029A>G	NP_001358522.1:p.Glu343=
NM_001371594.1:c.996A>G	NP_001358523.1:p.Glu332=
NM_001371595.1:c.861A>G	NP_001358524.1:p.Glu287=
NM_001371596.2:c.1143A>G MANE Select	NP_001358525.1:p.Glu381=
NM_152778.3:c.1143A>G	NP_689991.1:p.Glu381=
NM_152778.4:c.1143A>G	NP_689991.1:p.Glu381=