Canonical Allele Identifier: CA1922573256

Gene: MAT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80275006_80275007delinsAG , CM000672.2:g.80275006_80275007delinsAG	GRCh38
NC_000010.10:g.82034762_82034763delinsAG , CM000672.1:g.82034762_82034763delinsAG	GRCh37
NC_000010.9:g.82024742_82024743delinsAG	NCBI36
NG_008083.1:g.19672_19673delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372213.8:c.951+10_951+11delinsCT MANE Select	ENSP00000361287.3:n.951+10_951+11delinsCT
ENST00000372213.7:c.951+10_951+11delinsCT	ENSP00000361287.3:n.951+10_951+11delinsCT
ENST00000480845.1:n.183+10_183+11delinsCT
ENST00000485270.5:n.463+10_463+11delinsCT
NM_000429.2:c.951+10_951+11delinsCT	NP_000420.1:n.951+10_951+11delinsCT
XM_005269842.3:c.951+10_951+11delinsCT	XP_005269899.1:n.951+10_951+11delinsCT
XM_005269843.3:c.828+10_828+11delinsCT	XP_005269900.1:n.828+10_828+11delinsCT
NM_000429.3:c.951+10_951+11delinsCT MANE Select	NP_000420.1:n.951+10_951+11delinsCT