Canonical Allele Identifier: CA9232906

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12864885G>A , CM000681.2:g.12864885G>A GRCh38
NC_000019.9:g.12975699G>A , CM000681.1:g.12975699G>A GRCh37
NC_000019.8:g.12836699G>A NCBI36
NG_054729.1:g.35955G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251472.9:c.1443G>A (MAST1) MANE Select ENSP00000251472.3:p.Thr481=
ENST00000251472.8:c.1443G>A (MAST1) ENSP00000251472.3:p.Thr481=
ENST00000589040.1:n.498G>A (MAST1)
ENST00000589765.1:n.32+7824C>T (HOOK2)
NM_014975.2:c.1443G>A (MAST1) NP_055790.1:p.Thr481=
XM_011527805.1:c.1431G>A (MAST1) XP_011526107.1:p.Thr477=
XM_011527806.1:c.1155G>A (MAST1) XP_011526108.1:p.Thr385=
XM_011527807.1:c.915G>A (MAST1) XP_011526109.1:p.Thr305=
XM_011527808.1:c.111G>A (MAST1) XP_011526110.1:p.Thr37=
XM_011527805.2:c.1431G>A (MAST1) XP_011526107.1:p.Thr477=
XM_011527808.2:c.111G>A (MAST1) XP_011526110.1:p.Thr37=
NM_014975.3:c.1443G>A (MAST1) MANE Select NP_055790.1:p.Thr481=