Canonical Allele Identifier: CA4289028

Gene: MLXIPL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73596240C>T , CM000669.2:g.73596240C>T	GRCh38
NC_000007.13:g.73010570C>T , CM000669.1:g.73010570C>T	GRCh37
NC_000007.12:g.72648506C>T	NCBI36
NG_009307.1:g.33301G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313375.8:c.1971G>A MANE Select	ENSP00000320886.3:p.Ala657=
ENST00000313375.7:c.1971G>A	ENSP00000320886.3:p.Ala657=
ENST00000345114.9:c.1820G>A	ENSP00000343767.5:n.1820G>A
ENST00000354613.5:c.1965G>A	ENSP00000346629.1:p.Ala655=
ENST00000414749.6:c.1965G>A	ENSP00000412330.2:p.Ala655=
ENST00000429400.6:c.1971G>A	ENSP00000406296.2:p.Ala657=
ENST00000434326.5:c.1689G>A	ENSP00000392636.1:p.Ala563=
ENST00000467221.1:n.708G>A
NM_032951.2:c.1971G>A	NP_116569.1:p.Ala657=
NM_032952.2:c.1971G>A	NP_116570.1:p.Ala657=
NM_032953.2:c.1965G>A	NP_116571.1:p.Ala655=
NM_032954.2:c.1965G>A	NP_116572.1:p.Ala655=
XM_011516277.1:c.2166G>A	XP_011514579.1:p.Ala722=
XM_011516278.1:c.2163G>A	XP_011514580.1:p.Ala721=
XM_011516279.1:c.2166G>A	XP_011514581.1:p.Ala722=
XM_011516280.1:c.1470G>A	XP_011514582.1:p.Ala490=
XM_011516281.1:c.1143G>A	XP_011514583.1:p.Ala381=
XR_927474.1:n.2045G>A
XR_927475.1:n.1850G>A
NR_134541.1:n.1871G>A
XM_011516281.2:c.1143G>A	XP_011514583.1:p.Ala381=
XM_017012263.1:c.1062G>A	XP_016867752.1:p.Ala354=
XM_024446784.1:c.1140G>A	XP_024302552.1:p.Ala380=
XR_001744799.1:n.2045G>A
NM_032951.3:c.1971G>A MANE Select	NP_116569.1:p.Ala657=
NM_032952.3:c.1971G>A	NP_116570.1:p.Ala657=
NM_032953.3:c.1965G>A	NP_116571.1:p.Ala655=
NM_032954.3:c.1965G>A	NP_116572.1:p.Ala655=
NR_134541.2:n.1850G>A