Canonical Allele Identifier: CA2609912787
Gene: MAT1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80273974_80273979del , CM000672.2:g.80273974_80273979del GRCh38
NC_000010.10:g.82033730_82033735del , CM000672.1:g.82033730_82033735del GRCh37
NC_000010.9:g.82023710_82023715del NCBI36
NG_008083.1:g.20703_20708del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.1086-93_1086-88del MANE Select ENSP00000361287.3:n.1086-93_1086-88del
ENST00000372213.7:c.1086-93_1086-88del ENSP00000361287.3:n.1086-93_1086-88del
ENST00000480845.1:n.318-93_318-88del
ENST00000485270.5:n.598-93_598-88del
NM_000429.2:c.1086-93_1086-88del NP_000420.1:n.1086-93_1086-88del
XM_005269842.3:c.1086-93_1086-88del XP_005269899.1:n.1086-93_1086-88del
XM_005269843.3:c.963-93_963-88del XP_005269900.1:n.963-93_963-88del
NM_000429.3:c.1086-93_1086-88del MANE Select NP_000420.1:n.1086-93_1086-88del