Canonical Allele Identifier: CA1922577337
Gene: MAT1A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80273939T= , CM000672.2:g.80273939T= GRCh38
NC_000010.10:g.82033695T= , CM000672.1:g.82033695T= GRCh37
NC_000010.9:g.82023675T= NCBI36
NG_008083.1:g.20740A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.1086-56A= MANE Select ENSP00000361287.3:n.1086-56A=
ENST00000372213.7:c.1086-56A= ENSP00000361287.3:n.1086-56A=
ENST00000480845.1:n.318-56A=
ENST00000485270.5:n.598-56A=
NM_000429.2:c.1086-56A= NP_000420.1:n.1086-56A=
XM_005269842.3:c.1086-56A= XP_005269899.1:n.1086-56A=
XM_005269843.3:c.963-56A= XP_005269900.1:n.963-56A=
NM_000429.3:c.1086-56A= MANE Select NP_000420.1:n.1086-56A=
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