Canonical Allele Identifier: CA4289385

Gene: MLXIPL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73605728C>T , CM000669.2:g.73605728C>T	GRCh38
NC_000007.13:g.73020058C>T , CM000669.1:g.73020058C>T	GRCh37
NC_000007.12:g.72657994C>T	NCBI36
NG_009307.1:g.23813G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313375.8:c.861G>A MANE Select	ENSP00000320886.3:p.Thr287=
ENST00000313375.7:c.861G>A	ENSP00000320886.3:p.Thr287=
ENST00000345114.9:c.861G>A	ENSP00000343767.5:p.Thr287=
ENST00000354613.5:c.861G>A	ENSP00000346629.1:p.Thr287=
ENST00000414749.6:c.861G>A	ENSP00000412330.2:p.Thr287=
ENST00000429400.6:c.861G>A	ENSP00000406296.2:p.Thr287=
ENST00000434326.5:c.582G>A	ENSP00000392636.1:p.Thr194=
ENST00000453275.1:c.401-6033G>A	ENSP00000395172.1:n.401-6033G>A
ENST00000476404.5:n.956G>A
ENST00000488212.1:n.390G>A
NM_032951.2:c.861G>A	NP_116569.1:p.Thr287=
NM_032952.2:c.861G>A	NP_116570.1:p.Thr287=
NM_032953.2:c.861G>A	NP_116571.1:p.Thr287=
NM_032954.2:c.861G>A	NP_116572.1:p.Thr287=
XM_011516277.1:c.1056G>A	XP_011514579.1:p.Thr352=
XM_011516278.1:c.1056G>A	XP_011514580.1:p.Thr352=
XM_011516279.1:c.1056G>A	XP_011514581.1:p.Thr352=
XM_011516280.1:c.401-6033G>A	XP_011514582.1:n.401-6033G>A
XR_927474.1:n.1086G>A
XR_927475.1:n.891G>A
NR_134541.1:n.912G>A
XM_017012263.1:c.-20G>A	XP_016867752.1:n.-20G>A
XR_001744799.1:n.1086G>A
NM_032951.3:c.861G>A MANE Select	NP_116569.1:p.Thr287=
NM_032952.3:c.861G>A	NP_116570.1:p.Thr287=
NM_032953.3:c.861G>A	NP_116571.1:p.Thr287=
NM_032954.3:c.861G>A	NP_116572.1:p.Thr287=
NR_134541.2:n.891G>A