Canonical Allele Identifier: CA1922577942
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80280320T= , CM000672.2:g.80280320T= GRCh38
NC_000010.10:g.82040076T= , CM000672.1:g.82040076T= GRCh37
NC_000010.9:g.82030056T= NCBI36
NG_008083.1:g.14359A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.406-4A= MANE Select ENSP00000361287.3:n.406-4A=
ENST00000372213.7:c.406-4A= ENSP00000361287.3:n.406-4A=
ENST00000455001.1:c.217-4A= ENSP00000414961.1:n.217-4A=
NM_000429.2:c.406-4A= NP_000420.1:n.406-4A=
XM_005269842.3:c.406-4A= XP_005269899.1:n.406-4A=
XM_005269843.3:c.283-4A= XP_005269900.1:n.283-4A=
NM_000429.3:c.406-4A= MANE Select NP_000420.1:n.406-4A=