Canonical Allele Identifier: CA2842879632
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80274996T>C , CM000672.2:g.80274996T>C GRCh38
NC_000010.10:g.82034752T>C , CM000672.1:g.82034752T>C GRCh37
NC_000010.9:g.82024732T>C NCBI36
NG_008083.1:g.19683A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.951+21A>G MANE Select ENSP00000361287.3:n.951+21A>G
ENST00000372213.7:c.951+21A>G ENSP00000361287.3:n.951+21A>G
ENST00000480845.1:n.183+21A>G
ENST00000485270.5:n.463+21A>G
NM_000429.2:c.951+21A>G NP_000420.1:n.951+21A>G
XM_005269842.3:c.951+21A>G XP_005269899.1:n.951+21A>G
XM_005269843.3:c.828+21A>G XP_005269900.1:n.828+21A>G
NM_000429.3:c.951+21A>G MANE Select NP_000420.1:n.951+21A>G