Canonical Allele Identifier: CA505776202

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12864852C>G , CM000681.2:g.12864852C>G GRCh38
NC_000019.9:g.12975666C>G , CM000681.1:g.12975666C>G GRCh37
NC_000019.8:g.12836666C>G NCBI36
NG_054729.1:g.35922C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251472.9:c.1410C>G (MAST1) MANE Select ENSP00000251472.3:p.Pro470=
ENST00000251472.8:c.1410C>G (MAST1) ENSP00000251472.3:p.Pro470=
ENST00000589040.1:n.465C>G (MAST1)
ENST00000589765.1:n.32+7857G>C (HOOK2)
NM_014975.2:c.1410C>G (MAST1) NP_055790.1:p.Pro470=
XM_011527805.1:c.1398C>G (MAST1) XP_011526107.1:p.Pro466=
XM_011527806.1:c.1122C>G (MAST1) XP_011526108.1:p.Pro374=
XM_011527807.1:c.882C>G (MAST1) XP_011526109.1:p.Pro294=
XM_011527808.1:c.78C>G (MAST1) XP_011526110.1:p.Pro26=
XM_011527805.2:c.1398C>G (MAST1) XP_011526107.1:p.Pro466=
XM_011527808.2:c.78C>G (MAST1) XP_011526110.1:p.Pro26=
NM_014975.3:c.1410C>G (MAST1) MANE Select NP_055790.1:p.Pro470=