Canonical Allele Identifier: CA160068300

Gene: MLXIPL

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73612048C>T , CM000669.2:g.73612048C>T	GRCh38
NC_000007.13:g.73026378C>T , CM000669.1:g.73026378C>T	GRCh37
NC_000007.12:g.72664314C>T	NCBI36
NG_009307.1:g.17493G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456640.2:c.400+4023G>A	ENSP00000402615.2:n.400+4023G>A
ENST00000313375.8:c.400+4023G>A MANE Select	ENSP00000320886.3:n.400+4023G>A
ENST00000313375.7:c.400+4023G>A	ENSP00000320886.3:n.400+4023G>A
ENST00000345114.9:c.400+4023G>A	ENSP00000343767.5:n.400+4023G>A
ENST00000354613.5:c.400+4023G>A	ENSP00000346629.1:n.400+4023G>A
ENST00000414749.6:c.400+4023G>A	ENSP00000412330.2:n.400+4023G>A
ENST00000429400.6:c.400+4023G>A	ENSP00000406296.2:n.400+4023G>A
ENST00000434326.5:c.400+4023G>A	ENSP00000392636.1:n.400+4023G>A
ENST00000453275.1:c.400+4023G>A	ENSP00000395172.1:n.400+4023G>A
ENST00000456640.1:c.91+4023G>A	ENSP00000402615.1:n.91+4023G>A
NM_032951.2:c.400+4023G>A	NP_116569.1:n.400+4023G>A
NM_032952.2:c.400+4023G>A	NP_116570.1:n.400+4023G>A
NM_032953.2:c.400+4023G>A	NP_116571.1:n.400+4023G>A
NM_032954.2:c.400+4023G>A	NP_116572.1:n.400+4023G>A
XM_011516277.1:c.400+4023G>A	XP_011514579.1:n.400+4023G>A
XM_011516278.1:c.400+4023G>A	XP_011514580.1:n.400+4023G>A
XM_011516279.1:c.400+4023G>A	XP_011514581.1:n.400+4023G>A
XM_011516280.1:c.400+4023G>A	XP_011514582.1:n.400+4023G>A
XR_927474.1:n.430+4023G>A
XR_927475.1:n.430+4023G>A
NR_134541.1:n.451+4023G>A
XR_001744799.1:n.430+4023G>A
NM_032951.3:c.400+4023G>A MANE Select	NP_116569.1:n.400+4023G>A
NM_032952.3:c.400+4023G>A	NP_116570.1:n.400+4023G>A
NM_032953.3:c.400+4023G>A	NP_116571.1:n.400+4023G>A
NM_032954.3:c.400+4023G>A	NP_116572.1:n.400+4023G>A
NR_134541.2:n.430+4023G>A