Canonical Allele Identifier: CA1922573199

Gene: MAT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80274948_80274949delinsCT , CM000672.2:g.80274948_80274949delinsCT	GRCh38
NC_000010.10:g.82034704_82034705delinsCT , CM000672.1:g.82034704_82034705delinsCT	GRCh37
NC_000010.9:g.82024684_82024685delinsCT	NCBI36
NG_008083.1:g.19730_19731delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372213.8:c.951+68_951+69delinsAG MANE Select	ENSP00000361287.3:n.951+68_951+69delinsAG
ENST00000372213.7:c.951+68_951+69delinsAG	ENSP00000361287.3:n.951+68_951+69delinsAG
ENST00000480845.1:n.183+68_183+69delinsAG
ENST00000485270.5:n.463+68_463+69delinsAG
NM_000429.2:c.951+68_951+69delinsAG	NP_000420.1:n.951+68_951+69delinsAG
XM_005269842.3:c.951+68_951+69delinsAG	XP_005269899.1:n.951+68_951+69delinsAG
XM_005269843.3:c.828+68_828+69delinsAG	XP_005269900.1:n.828+68_828+69delinsAG
NM_000429.3:c.951+68_951+69delinsAG MANE Select	NP_000420.1:n.951+68_951+69delinsAG