Canonical Allele Identifier: CA4288934

Gene: MLXIPL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73595675C>T , CM000669.2:g.73595675C>T	GRCh38
NC_000007.13:g.73010005C>T , CM000669.1:g.73010005C>T	GRCh37
NC_000007.12:g.72647941C>T	NCBI36
NG_009307.1:g.33866G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313375.8:c.2272G>A MANE Select	ENSP00000320886.3:p.Val758Ile
ENST00000313375.7:c.2272G>A	ENSP00000320886.3:p.Val758Ile
ENST00000345114.9:c.2121G>A	ENSP00000343767.5:n.2121G>A
ENST00000354613.5:c.2209G>A	ENSP00000346629.1:p.Val737Ile
ENST00000414749.6:c.2266G>A	ENSP00000412330.2:p.Val756Ile
ENST00000429400.6:c.2215G>A	ENSP00000406296.2:p.Val739Ile
ENST00000434326.5:c.1990G>A	ENSP00000392636.1:p.Val664Ile
NM_032951.2:c.2272G>A	NP_116569.1:p.Val758Ile
NM_032952.2:c.2215G>A	NP_116570.1:p.Val739Ile
NM_032953.2:c.2266G>A	NP_116571.1:p.Val756Ile
NM_032954.2:c.2209G>A	NP_116572.1:p.Val737Ile
XM_011516277.1:c.2467G>A	XP_011514579.1:p.Val823Ile
XM_011516278.1:c.2464G>A	XP_011514580.1:p.Val822Ile
XM_011516279.1:c.2413G>A	XP_011514581.1:p.Val805Ile
XM_011516280.1:c.1771G>A	XP_011514582.1:p.Val591Ile
XM_011516281.1:c.1444G>A	XP_011514583.1:p.Val482Ile
XR_927475.1:n.2151G>A
NR_134541.1:n.2172G>A
XM_011516281.2:c.1444G>A	XP_011514583.1:p.Val482Ile
XM_017012263.1:c.1363G>A	XP_016867752.1:p.Val455Ile
XM_024446784.1:c.1441G>A	XP_024302552.1:p.Val481Ile
XR_001744799.1:n.2346G>A
NM_032951.3:c.2272G>A MANE Select	NP_116569.1:p.Val758Ile
NM_032952.3:c.2215G>A	NP_116570.1:p.Val739Ile
NM_032953.3:c.2266G>A	NP_116571.1:p.Val756Ile
NM_032954.3:c.2209G>A	NP_116572.1:p.Val737Ile
NR_134541.2:n.2151G>A