Canonical Allele Identifier: CA367825015

Gene: MLXIPL

Linked Data

• MyVariant Identifiers: chr7:g.73013908A>G (hg19) ; chr7:g.73599578A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73599578A>G , CM000669.2:g.73599578A>G	GRCh38
NC_000007.13:g.73013908A>G , CM000669.1:g.73013908A>G	GRCh37
NC_000007.12:g.72651844A>G	NCBI36
NG_009307.1:g.29963T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000313375.8:c.1019T>C MANE Select	ENSP00000320886.3:p.Val340Ala
ENST00000313375.7:c.1019T>C	ENSP00000320886.3:p.Val340Ala
ENST00000345114.9:c.1019T>C	ENSP00000343767.5:p.Val340Ala
ENST00000354613.5:c.1019T>C	ENSP00000346629.1:p.Val340Ala
ENST00000414749.6:c.1019T>C	ENSP00000412330.2:p.Val340Ala
ENST00000429400.6:c.1019T>C	ENSP00000406296.2:p.Val340Ala
ENST00000434326.5:c.740T>C	ENSP00000392636.1:p.Val247Ala
ENST00000453275.1:c.518T>C	ENSP00000395172.1:p.Val173Ala
ENST00000476404.5:n.1114T>C
NM_032951.2:c.1019T>C	NP_116569.1:p.Val340Ala
NM_032952.2:c.1019T>C	NP_116570.1:p.Val340Ala
NM_032953.2:c.1019T>C	NP_116571.1:p.Val340Ala
NM_032954.2:c.1019T>C	NP_116572.1:p.Val340Ala
XM_011516277.1:c.1214T>C	XP_011514579.1:p.Val405Ala
XM_011516278.1:c.1214T>C	XP_011514580.1:p.Val405Ala
XM_011516279.1:c.1214T>C	XP_011514581.1:p.Val405Ala
XM_011516280.1:c.518T>C	XP_011514582.1:p.Val173Ala
XM_011516281.1:c.191T>C	XP_011514583.1:p.Val64Ala
XR_927474.1:n.1244T>C
XR_927475.1:n.1049T>C
NR_134541.1:n.1070T>C
XM_011516281.2:c.191T>C	XP_011514583.1:p.Val64Ala
XM_017012263.1:c.110T>C	XP_016867752.1:p.Val37Ala
XM_024446784.1:c.191T>C	XP_024302552.1:p.Val64Ala
XR_001744799.1:n.1244T>C
NM_032951.3:c.1019T>C MANE Select	NP_116569.1:p.Val340Ala
NM_032952.3:c.1019T>C	NP_116570.1:p.Val340Ala
NM_032953.3:c.1019T>C	NP_116571.1:p.Val340Ala
NM_032954.3:c.1019T>C	NP_116572.1:p.Val340Ala
NR_134541.2:n.1049T>C