Canonical Allele Identifier: CA2545355389
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275185_80275186del , CM000672.2:g.80275185_80275186del GRCh38
NC_000010.10:g.82034941_82034942del , CM000672.1:g.82034941_82034942del GRCh37
NC_000010.9:g.82024921_82024922del NCBI36
NG_008083.1:g.19493_19494del

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.782_783del MANE Select ENSP00000361287.3:p.Val261AspfsTer4
ENST00000372213.7:c.782_783del ENSP00000361287.3:p.Val261AspfsTer4
ENST00000480845.1:n.14_15del
ENST00000485270.5:n.294_295del
NM_000429.2:c.782_783del NP_000420.1:p.Val261AspfsTer4
XM_005269842.3:c.782_783del XP_005269899.1:p.Val261AspfsTer4
XM_005269843.3:c.659_660del XP_005269900.1:p.Val220AspfsTer4
NM_000429.3:c.782_783del MANE Select NP_000420.1:p.Val261AspfsTer4