Canonical Allele Identifier: CA1922578042
Gene: MAT1A HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80280507A= , CM000672.2:g.80280507A= GRCh38
NC_000010.10:g.82040263A= , CM000672.1:g.82040263A= GRCh37
NC_000010.9:g.82030243A= NCBI36
NG_008083.1:g.14172T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.405+173T= MANE Select ENSP00000361287.3:n.405+173T=
ENST00000372213.7:c.405+173T= ENSP00000361287.3:n.405+173T=
ENST00000455001.1:c.216+173T= ENSP00000414961.1:n.216+173T=
NM_000429.2:c.405+173T= NP_000420.1:n.405+173T=
XM_005269842.3:c.405+173T= XP_005269899.1:n.405+173T=
XM_005269843.3:c.282+173T= XP_005269900.1:n.282+173T=
NM_000429.3:c.405+173T= MANE Select NP_000420.1:n.405+173T=
Search 100 bp 5'
Search 100 bp 3'