Canonical Allele Identifier: CA1717122309

Gene: MLXIPL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73593613G= , CM000669.2:g.73593613G=	GRCh38
NC_000007.13:g.73007943G= , CM000669.1:g.73007943G=	GRCh37
NC_000007.12:g.72645879G=	NCBI36
NG_009307.1:g.35928C=

Transcript Alleles

HGVS	Amino-acid Change
NM_032951.3:c.*252C= MANE Select	NP_116569.1:n.*252C=
ENST00000313375.8:c.*252C= MANE Select	ENSP00000320886.3:n.*252C=
NM_032951.2:c.*252C=	NP_116569.1:n.*252C=
NM_032952.2:c.*252C=	NP_116570.1:n.*252C=
NM_032952.3:c.*252C=	NP_116570.1:n.*252C=
NM_032953.2:c.*252C=	NP_116571.1:n.*252C=
NM_032953.3:c.*252C=	NP_116571.1:n.*252C=
NM_032954.2:c.*252C=	NP_116572.1:n.*252C=
NM_032954.3:c.*252C=	NP_116572.1:n.*252C=
NR_134541.1:n.2711C=
NR_134541.2:n.2690C=
ENST00000313375.7:c.*252C=	ENSP00000320886.3:n.*252C=
ENST00000345114.9:c.2660C=	ENSP00000343767.5:n.2660C=
ENST00000354613.5:c.*252C=	ENSP00000346629.1:n.*252C=
ENST00000414749.6:c.2805C=	ENSP00000412330.2:n.2805C=
ENST00000429400.6:c.2754C=	ENSP00000406296.2:n.2754C=
ENST00000434326.5:c.*653C=	ENSP00000392636.1:n.*653C=
XM_011516277.1:c.*252C=	XP_011514579.1:n.*252C=
XM_011516278.1:c.*252C=	XP_011514580.1:n.*252C=
XM_011516279.1:c.*252C=	XP_011514581.1:n.*252C=
XM_011516280.1:c.*252C=	XP_011514582.1:n.*252C=
XM_011516281.1:c.*252C=	XP_011514583.1:n.*252C=
XM_011516281.2:c.*252C=	XP_011514583.1:n.*252C=
XM_017012263.1:c.*252C=	XP_016867752.1:n.*252C=
XM_024446784.1:c.*252C=	XP_024302552.1:n.*252C=
XR_001744799.1:n.2885C=
XR_927475.1:n.2690C=