Canonical Allele Identifier: CA4288968

Gene: MLXIPL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73595861C>T , CM000669.2:g.73595861C>T	GRCh38
NC_000007.13:g.73010191C>T , CM000669.1:g.73010191C>T	GRCh37
NC_000007.12:g.72648127C>T	NCBI36
NG_009307.1:g.33680G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313375.8:c.2167G>A MANE Select	ENSP00000320886.3:p.Glu723Lys
ENST00000313375.7:c.2167G>A	ENSP00000320886.3:p.Glu723Lys
ENST00000345114.9:c.2016G>A	ENSP00000343767.5:n.2016G>A
ENST00000354613.5:c.2104G>A	ENSP00000346629.1:p.Glu702Lys
ENST00000414749.6:c.2161G>A	ENSP00000412330.2:p.Glu721Lys
ENST00000429400.6:c.2110G>A	ENSP00000406296.2:p.Glu704Lys
ENST00000434326.5:c.1885G>A	ENSP00000392636.1:p.Glu629Lys
NM_032951.2:c.2167G>A	NP_116569.1:p.Glu723Lys
NM_032952.2:c.2110G>A	NP_116570.1:p.Glu704Lys
NM_032953.2:c.2161G>A	NP_116571.1:p.Glu721Lys
NM_032954.2:c.2104G>A	NP_116572.1:p.Glu702Lys
XM_011516277.1:c.2362G>A	XP_011514579.1:p.Glu788Lys
XM_011516278.1:c.2359G>A	XP_011514580.1:p.Glu787Lys
XM_011516279.1:c.2308G>A	XP_011514581.1:p.Glu770Lys
XM_011516280.1:c.1666G>A	XP_011514582.1:p.Glu556Lys
XM_011516281.1:c.1339G>A	XP_011514583.1:p.Glu447Lys
XR_927475.1:n.2046G>A
NR_134541.1:n.2067G>A
XM_011516281.2:c.1339G>A	XP_011514583.1:p.Glu447Lys
XM_017012263.1:c.1258G>A	XP_016867752.1:p.Glu420Lys
XM_024446784.1:c.1336G>A	XP_024302552.1:p.Glu446Lys
XR_001744799.1:n.2241G>A
NM_032951.3:c.2167G>A MANE Select	NP_116569.1:p.Glu723Lys
NM_032952.3:c.2110G>A	NP_116570.1:p.Glu704Lys
NM_032953.3:c.2161G>A	NP_116571.1:p.Glu721Lys
NM_032954.3:c.2104G>A	NP_116572.1:p.Glu702Lys
NR_134541.2:n.2046G>A