Canonical Allele Identifier: CA4288895

Gene: MLXIPL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73594286C>T , CM000669.2:g.73594286C>T	GRCh38
NC_000007.13:g.73008616C>T , CM000669.1:g.73008616C>T	GRCh37
NC_000007.12:g.72646552C>T	NCBI36
NG_009307.1:g.35255G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313375.8:c.2428G>A MANE Select	ENSP00000320886.3:p.Ala810Thr
ENST00000313375.7:c.2428G>A	ENSP00000320886.3:p.Ala810Thr
ENST00000345114.9:c.2277G>A	ENSP00000343767.5:n.2277G>A
ENST00000354613.5:c.2365G>A	ENSP00000346629.1:p.Ala789Thr
ENST00000414749.6:c.2422G>A	ENSP00000412330.2:p.Ala808Thr
ENST00000429400.6:c.2371G>A	ENSP00000406296.2:p.Ala791Thr
ENST00000434326.5:c.2146G>A	ENSP00000392636.1:p.Ala716Thr
NM_032951.2:c.2428G>A	NP_116569.1:p.Ala810Thr
NM_032952.2:c.2371G>A	NP_116570.1:p.Ala791Thr
NM_032953.2:c.2422G>A	NP_116571.1:p.Ala808Thr
NM_032954.2:c.2365G>A	NP_116572.1:p.Ala789Thr
XM_011516277.1:c.2623G>A	XP_011514579.1:p.Ala875Thr
XM_011516278.1:c.2620G>A	XP_011514580.1:p.Ala874Thr
XM_011516279.1:c.2569G>A	XP_011514581.1:p.Ala857Thr
XM_011516280.1:c.1927G>A	XP_011514582.1:p.Ala643Thr
XM_011516281.1:c.1600G>A	XP_011514583.1:p.Ala534Thr
XR_927475.1:n.2307G>A
NR_134541.1:n.2328G>A
XM_011516281.2:c.1600G>A	XP_011514583.1:p.Ala534Thr
XM_017012263.1:c.1519G>A	XP_016867752.1:p.Ala507Thr
XM_024446784.1:c.1597G>A	XP_024302552.1:p.Ala533Thr
XR_001744799.1:n.2502G>A
NM_032951.3:c.2428G>A MANE Select	NP_116569.1:p.Ala810Thr
NM_032952.3:c.2371G>A	NP_116570.1:p.Ala791Thr
NM_032953.3:c.2422G>A	NP_116571.1:p.Ala808Thr
NM_032954.3:c.2365G>A	NP_116572.1:p.Ala789Thr
NR_134541.2:n.2307G>A