Canonical Allele Identifier: CA367825028

Gene: MLXIPL

Linked Data

• MyVariant Identifiers: chr7:g.73013910C>A (hg19) ; chr7:g.73599580C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73599580C>A , CM000669.2:g.73599580C>A	GRCh38
NC_000007.13:g.73013910C>A , CM000669.1:g.73013910C>A	GRCh37
NC_000007.12:g.72651846C>A	NCBI36
NG_009307.1:g.29961G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000313375.8:c.1017G>T MANE Select	ENSP00000320886.3:p.Glu339Asp
ENST00000313375.7:c.1017G>T	ENSP00000320886.3:p.Glu339Asp
ENST00000345114.9:c.1017G>T	ENSP00000343767.5:p.Glu339Asp
ENST00000354613.5:c.1017G>T	ENSP00000346629.1:p.Glu339Asp
ENST00000414749.6:c.1017G>T	ENSP00000412330.2:p.Glu339Asp
ENST00000429400.6:c.1017G>T	ENSP00000406296.2:p.Glu339Asp
ENST00000434326.5:c.738G>T	ENSP00000392636.1:p.Glu246Asp
ENST00000453275.1:c.516G>T	ENSP00000395172.1:p.Glu172Asp
ENST00000476404.5:n.1112G>T
NM_032951.2:c.1017G>T	NP_116569.1:p.Glu339Asp
NM_032952.2:c.1017G>T	NP_116570.1:p.Glu339Asp
NM_032953.2:c.1017G>T	NP_116571.1:p.Glu339Asp
NM_032954.2:c.1017G>T	NP_116572.1:p.Glu339Asp
XM_011516277.1:c.1212G>T	XP_011514579.1:p.Glu404Asp
XM_011516278.1:c.1212G>T	XP_011514580.1:p.Glu404Asp
XM_011516279.1:c.1212G>T	XP_011514581.1:p.Glu404Asp
XM_011516280.1:c.516G>T	XP_011514582.1:p.Glu172Asp
XM_011516281.1:c.189G>T	XP_011514583.1:p.Glu63Asp
XR_927474.1:n.1242G>T
XR_927475.1:n.1047G>T
NR_134541.1:n.1068G>T
XM_011516281.2:c.189G>T	XP_011514583.1:p.Glu63Asp
XM_017012263.1:c.108G>T	XP_016867752.1:p.Glu36Asp
XM_024446784.1:c.189G>T	XP_024302552.1:p.Glu63Asp
XR_001744799.1:n.1242G>T
NM_032951.3:c.1017G>T MANE Select	NP_116569.1:p.Glu339Asp
NM_032952.3:c.1017G>T	NP_116570.1:p.Glu339Asp
NM_032953.3:c.1017G>T	NP_116571.1:p.Glu339Asp
NM_032954.3:c.1017G>T	NP_116572.1:p.Glu339Asp
NR_134541.2:n.1047G>T