Canonical Allele Identifier: CA404264877

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12852176G>A , CM000681.2:g.12852176G>A GRCh38
NC_000019.9:g.12962990G>A , CM000681.1:g.12962990G>A GRCh37
NC_000019.8:g.12823990G>A NCBI36
NG_054729.1:g.23246G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000591495.6:c.926G>A (MAST1) ENSP00000466470.1:p.Gly309Asp
ENST00000699746.1:c.476G>A (MAST1) ENSP00000514556.1:p.Gly159Asp
ENST00000251472.9:c.938G>A (MAST1) MANE Select ENSP00000251472.3:p.Gly313Asp
ENST00000251472.8:c.938G>A (MAST1) ENSP00000251472.3:p.Gly313Asp
ENST00000588379.5:c.798G>A (MAST1)
ENST00000589765.1:n.32+20533C>T (HOOK2)
ENST00000591495.5:c.926G>A (MAST1) ENSP00000466470.1:p.Gly309Asp
NM_014975.2:c.938G>A (MAST1) NP_055790.1:p.Gly313Asp
XM_011527805.1:c.926G>A (MAST1) XP_011526107.1:p.Gly309Asp
XM_011527806.1:c.650G>A (MAST1) XP_011526108.1:p.Gly217Asp
XM_011527807.1:c.410G>A (MAST1) XP_011526109.1:p.Gly137Asp
XM_011527805.2:c.926G>A (MAST1) XP_011526107.1:p.Gly309Asp
NM_014975.3:c.938G>A (MAST1) MANE Select NP_055790.1:p.Gly313Asp