Canonical Allele Identifier: CA2574455310
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80274923_80274924insT , CM000672.2:g.80274923_80274924insT GRCh38
NC_000010.10:g.82034679_82034680insT , CM000672.1:g.82034679_82034680insT GRCh37
NC_000010.9:g.82024659_82024660insT NCBI36
NG_008083.1:g.19755_19756insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.951+93_951+94insA MANE Select ENSP00000361287.3:n.951+93_951+94insA
ENST00000372213.7:c.951+93_951+94insA ENSP00000361287.3:n.951+93_951+94insA
ENST00000480845.1:n.183+93_183+94insA
ENST00000485270.5:n.463+93_463+94insA
NM_000429.2:c.951+93_951+94insA NP_000420.1:n.951+93_951+94insA
XM_005269842.3:c.951+93_951+94insA XP_005269899.1:n.951+93_951+94insA
XM_005269843.3:c.828+93_828+94insA XP_005269900.1:n.828+93_828+94insA
NM_000429.3:c.951+93_951+94insA MANE Select NP_000420.1:n.951+93_951+94insA