Canonical Allele Identifier: CA1922577284
Gene: MAT1A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80273904A= , CM000672.2:g.80273904A= GRCh38
NC_000010.10:g.82033660A= , CM000672.1:g.82033660A= GRCh37
NC_000010.9:g.82023640A= NCBI36
NG_008083.1:g.20775T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.1086-21T= MANE Select ENSP00000361287.3:n.1086-21T=
ENST00000372213.7:c.1086-21T= ENSP00000361287.3:n.1086-21T=
ENST00000480845.1:n.318-21T=
ENST00000485270.5:n.598-21T=
NM_000429.2:c.1086-21T= NP_000420.1:n.1086-21T=
XM_005269842.3:c.1086-21T= XP_005269899.1:n.1086-21T=
XM_005269843.3:c.963-21T= XP_005269900.1:n.963-21T=
NM_000429.3:c.1086-21T= MANE Select NP_000420.1:n.1086-21T=
Search 100 bp 5'
Search 100 bp 3'