Canonical Allele Identifier: CA367828878

Gene: MLXIPL

Linked Data

• gnomAD v4: 7-73606095-G-T
• MyVariant Identifiers: chr7:g.73020425G>T (hg19) ; chr7:g.73606095G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73606095G>T , CM000669.2:g.73606095G>T	GRCh38
NC_000007.13:g.73020425G>T , CM000669.1:g.73020425G>T	GRCh37
NC_000007.12:g.72658361G>T	NCBI36
NG_009307.1:g.23446C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456640.2:c.830C>A	ENSP00000402615.2:p.Pro277Gln
ENST00000313375.8:c.635C>A MANE Select	ENSP00000320886.3:p.Pro212Gln
ENST00000313375.7:c.635C>A	ENSP00000320886.3:p.Pro212Gln
ENST00000345114.9:c.635C>A	ENSP00000343767.5:p.Pro212Gln
ENST00000354613.5:c.635C>A	ENSP00000346629.1:p.Pro212Gln
ENST00000414749.6:c.635C>A	ENSP00000412330.2:p.Pro212Gln
ENST00000429400.6:c.635C>A	ENSP00000406296.2:p.Pro212Gln
ENST00000434326.5:c.526-170C>A	ENSP00000392636.1:n.526-170C>A
ENST00000453275.1:c.401-6400C>A	ENSP00000395172.1:n.401-6400C>A
ENST00000456640.1:c.521C>A	ENSP00000402615.1:p.Pro174Gln
ENST00000476404.5:n.730C>A
ENST00000488212.1:n.164C>A
NM_032951.2:c.635C>A	NP_116569.1:p.Pro212Gln
NM_032952.2:c.635C>A	NP_116570.1:p.Pro212Gln
NM_032953.2:c.635C>A	NP_116571.1:p.Pro212Gln
NM_032954.2:c.635C>A	NP_116572.1:p.Pro212Gln
XM_011516277.1:c.830C>A	XP_011514579.1:p.Pro277Gln
XM_011516278.1:c.830C>A	XP_011514580.1:p.Pro277Gln
XM_011516279.1:c.830C>A	XP_011514581.1:p.Pro277Gln
XM_011516280.1:c.401-6400C>A	XP_011514582.1:n.401-6400C>A
XR_927474.1:n.860C>A
XR_927475.1:n.665C>A
NR_134541.1:n.686C>A
XR_001744799.1:n.860C>A
NM_032951.3:c.635C>A MANE Select	NP_116569.1:p.Pro212Gln
NM_032952.3:c.635C>A	NP_116570.1:p.Pro212Gln
NM_032953.3:c.635C>A	NP_116571.1:p.Pro212Gln
NM_032954.3:c.635C>A	NP_116572.1:p.Pro212Gln
NR_134541.2:n.665C>A