Canonical Allele Identifier: CA2609912788
Gene: MAT1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80273974del , CM000672.2:g.80273974del GRCh38
NC_000010.10:g.82033730del , CM000672.1:g.82033730del GRCh37
NC_000010.9:g.82023710del NCBI36
NG_008083.1:g.20705del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.1086-91del MANE Select ENSP00000361287.3:n.1086-91del
ENST00000372213.7:c.1086-91del ENSP00000361287.3:n.1086-91del
ENST00000480845.1:n.318-91del
ENST00000485270.5:n.598-91del
NM_000429.2:c.1086-91del NP_000420.1:n.1086-91del
XM_005269842.3:c.1086-91del XP_005269899.1:n.1086-91del
XM_005269843.3:c.963-91del XP_005269900.1:n.963-91del
NM_000429.3:c.1086-91del MANE Select NP_000420.1:n.1086-91del