Canonical Allele Identifier: CA4289226

Gene: MLXIPL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73597271G>A , CM000669.2:g.73597271G>A	GRCh38
NC_000007.13:g.73011601G>A , CM000669.1:g.73011601G>A	GRCh37
NC_000007.12:g.72649537G>A	NCBI36
NG_009307.1:g.32270C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313375.8:c.1514C>T MANE Select	ENSP00000320886.3:p.Ala505Val
ENST00000313375.7:c.1514C>T	ENSP00000320886.3:p.Ala505Val
ENST00000345114.9:c.1514C>T	ENSP00000343767.5:p.Ala505Val
ENST00000354613.5:c.1514C>T	ENSP00000346629.1:p.Ala505Val
ENST00000414749.6:c.1514C>T	ENSP00000412330.2:p.Ala505Val
ENST00000429400.6:c.1514C>T	ENSP00000406296.2:p.Ala505Val
ENST00000434326.5:c.1235C>T	ENSP00000392636.1:p.Ala412Val
ENST00000467221.1:n.92C>T
ENST00000476404.5:n.1609C>T
NM_032951.2:c.1514C>T	NP_116569.1:p.Ala505Val
NM_032952.2:c.1514C>T	NP_116570.1:p.Ala505Val
NM_032953.2:c.1514C>T	NP_116571.1:p.Ala505Val
NM_032954.2:c.1514C>T	NP_116572.1:p.Ala505Val
XM_011516277.1:c.1709C>T	XP_011514579.1:p.Ala570Val
XM_011516278.1:c.1709C>T	XP_011514580.1:p.Ala570Val
XM_011516279.1:c.1709C>T	XP_011514581.1:p.Ala570Val
XM_011516280.1:c.1013C>T	XP_011514582.1:p.Ala338Val
XM_011516281.1:c.686C>T	XP_011514583.1:p.Ala229Val
XR_927474.1:n.1739C>T
XR_927475.1:n.1544C>T
NR_134541.1:n.1565C>T
XM_011516281.2:c.686C>T	XP_011514583.1:p.Ala229Val
XM_017012263.1:c.605C>T	XP_016867752.1:p.Ala202Val
XM_024446784.1:c.686C>T	XP_024302552.1:p.Ala229Val
XR_001744799.1:n.1739C>T
NM_032951.3:c.1514C>T MANE Select	NP_116569.1:p.Ala505Val
NM_032952.3:c.1514C>T	NP_116570.1:p.Ala505Val
NM_032953.3:c.1514C>T	NP_116571.1:p.Ala505Val
NM_032954.3:c.1514C>T	NP_116572.1:p.Ala505Val
NR_134541.2:n.1544C>T