Canonical Allele Identifier: CA2323596471
Community Standard Title: NM_014975.3(MAST1):c.-1C=

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12838572C= , CM000681.2:g.12838572C= GRCh38
NC_000019.9:g.12949386C= , CM000681.1:g.12949386C= GRCh37
NC_000019.8:g.12810386C= NCBI36
NG_054729.1:g.9642C=

Transcript Alleles

HGVS Amino-acid Change
NM_014975.3:c.-1C= (MAST1) MANE Select NP_055790.1:n.-1C=
ENST00000251472.9:c.-1C= (MAST1) MANE Select ENSP00000251472.3:n.-1C=
NM_014975.2:c.-1C= (MAST1) NP_055790.1:n.-1C=
ENST00000251472.8:c.-1C= (MAST1) ENSP00000251472.3:n.-1C=
ENST00000589765.1:n.33-12072G= (HOOK2)
ENST00000590883.1:n.100C= (MAST1)
ENST00000591495.5:c.71+272C= (MAST1) ENSP00000466470.1:n.71+272C=
ENST00000591495.6:c.71+272C= (MAST1) ENSP00000466470.1:n.71+272C=
XM_011527805.1:c.71+272C= (MAST1) XP_011526107.1:n.71+272C=
XM_011527805.2:c.71+272C= (MAST1) XP_011526107.1:n.71+272C=
XM_011527806.1:c.39+4566C= (MAST1) XP_011526108.1:n.39+4566C=