Canonical Allele Identifier: CA1492804053

Gene: MFSD8

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.127921567A= , CM000666.2:g.127921567A=	GRCh38
NC_000004.11:g.128842722A= , CM000666.1:g.128842722A=	GRCh37
NC_000004.10:g.129062172A=	NCBI36
NG_008657.1:g.49418T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296468.8:c.1307T=	ENSP00000296468.3:p.Met436=
ENST00000509826.2:c.*628T=	ENSP00000421176.2:n.*628T=
ENST00000513559.6:c.1025T=	ENSP00000425000.2:p.Met342=
ENST00000515130.6:c.*192T=	ENSP00000493056.1:n.*192T=
ENST00000641025.1:c.*192T=	ENSP00000493346.1:n.*192T=
ENST00000641092.1:c.*192T=	ENSP00000493392.1:n.*192T=
ENST00000641133.1:c.*621T=	ENSP00000493192.1:n.*621T=
ENST00000641146.1:n.1173T=
ENST00000641147.1:c.857T=	ENSP00000493133.1:p.Met286=
ENST00000641178.1:c.1172T=	ENSP00000492989.1:p.Met391=
ENST00000641186.1:c.1193T=	ENSP00000493347.1:p.Met398=
ENST00000641228.1:c.*192T=	ENSP00000493194.1:n.*192T=
ENST00000641332.1:c.*368T=	ENSP00000493397.1:n.*368T=
ENST00000641340.1:c.*436T=	ENSP00000493191.1:n.*436T=
ENST00000641388.1:n.554T=
ENST00000641393.1:c.857T=	ENSP00000493197.1:p.Met286=
ENST00000641397.1:c.*192T=	ENSP00000493406.1:n.*192T=
ENST00000641413.1:c.232T=
ENST00000641434.1:c.1307T=	ENSP00000493279.1:p.Met436=
ENST00000641464.1:c.*540T=	ENSP00000493438.1:n.*540T=
ENST00000641482.1:c.*192T=	ENSP00000493277.1:n.*192T=
ENST00000641508.1:c.*540T=	ENSP00000493209.1:n.*540T=
ENST00000641509.1:c.992T=	ENSP00000493459.1:p.Met331=
ENST00000641590.1:c.*192T=	ENSP00000493132.1:n.*192T=
ENST00000641658.1:c.*472T=	ENSP00000492987.1:n.*472T=
ENST00000641686.2:c.1307T= MANE Select	ENSP00000493218.2:p.Met436=
ENST00000641690.1:c.1106T=	ENSP00000492966.1:p.Met369=
ENST00000641742.1:c.*472T=	ENSP00000493315.1:n.*472T=
ENST00000641748.1:c.1307T=	ENSP00000493330.1:p.Met436=
ENST00000641753.1:c.1134T=
ENST00000641774.1:c.*559T=	ENSP00000492960.1:n.*559T=
ENST00000641830.1:c.539T=
ENST00000641843.1:c.*368T=	ENSP00000493174.1:n.*368T=
ENST00000641869.1:c.508T=
ENST00000641870.1:c.*368T=	ENSP00000493044.1:n.*368T=
ENST00000641882.1:c.*472T=	ENSP00000493301.1:n.*472T=
ENST00000641928.1:c.*436T=	ENSP00000493418.1:n.*436T=
ENST00000641949.1:c.554-731T=	ENSP00000492891.1:n.554-731T=
ENST00000642012.1:n.1171T=
ENST00000642034.1:c.*192T=	ENSP00000493285.1:n.*192T=
ENST00000642042.1:c.1307T=	ENSP00000493260.1:p.Met436=
ENST00000642078.1:c.*368T=	ENSP00000492885.1:n.*368T=
ENST00000296468.7:c.1307T=	ENSP00000296468.3:p.Met436=
ENST00000504126.1:n.335T=
ENST00000513559.5:c.1172T=	ENSP00000425000.1:p.Met391=
ENST00000515130.5:n.1649T=
NM_152778.2:c.1307T=	NP_689991.1:p.Met436=
XM_005262893.1:c.1307T=	XP_005262950.1:p.Met436=
XM_005262896.1:c.1160T=	XP_005262953.1:p.Met387=
XM_005262897.1:c.1106T=	XP_005262954.1:p.Met369=
XM_005262898.2:c.*192T=	XP_005262955.1:n.*192T=
XM_011531830.1:c.1193T=	XP_011530132.1:p.Met398=
XM_011531831.1:c.992T=	XP_011530133.1:p.Met331=
XM_011531832.1:c.*192T=	XP_011530134.1:n.*192T=
XR_938717.1:n.1384T=
NM_001363520.1:c.1106T=	NP_001350449.1:p.Met369=
NM_001363521.1:c.992T=	NP_001350450.1:p.Met331=
XM_005262898.3:c.*192T=	XP_005262955.1:n.*192T=
XM_017007989.1:c.*192T=	XP_016863478.1:n.*192T=
XM_024453981.1:c.1172T=	XP_024309749.1:p.Met391=
XM_024453982.1:c.1058T=	XP_024309750.1:p.Met353=
XM_024453983.1:c.857T=	XP_024309751.1:p.Met286=
XR_001741194.1:n.1280T=
XR_001741195.1:n.1166T=
XR_001741196.1:n.1079T=
XR_001741197.1:n.1239T=
XR_001741198.2:n.1135T=
XR_001741199.1:n.1135T=
XR_938717.2:n.1384T=
NM_001363520.2:c.1106T=	NP_001350449.1:p.Met369=
NM_001363521.2:c.992T=	NP_001350450.1:p.Met331=
NM_001371590.1:c.1172T=	NP_001358519.1:p.Met391=
NM_001371591.1:c.1307T=	NP_001358520.1:p.Met436=
NM_001371592.1:c.1313T=	NP_001358521.1:p.Met438=
NM_001371593.1:c.1193T=	NP_001358522.1:p.Met398=
NM_001371594.1:c.1160T=	NP_001358523.1:p.Met387=
NM_001371595.1:c.1025T=	NP_001358524.1:p.Met342=
NM_001371596.2:c.1307T= MANE Select	NP_001358525.1:p.Met436=
NM_152778.3:c.1307T=	NP_689991.1:p.Met436=
NM_152778.4:c.1307T=	NP_689991.1:p.Met436=