Canonical Allele Identifier: CA1922574423
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80276312C= , CM000672.2:g.80276312C= GRCh38
NC_000010.10:g.82036068C= , CM000672.1:g.82036068C= GRCh37
NC_000010.9:g.82026048C= NCBI36
NG_008083.1:g.18367G=

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.768+64G= MANE Select ENSP00000361287.3:n.768+64G=
ENST00000372213.7:c.768+64G= ENSP00000361287.3:n.768+64G=
NM_000429.2:c.768+64G= NP_000420.1:n.768+64G=
XM_005269842.3:c.768+64G= XP_005269899.1:n.768+64G=
XM_005269843.3:c.645+64G= XP_005269900.1:n.645+64G=
NM_000429.3:c.768+64G= MANE Select NP_000420.1:n.768+64G=