Canonical Allele Identifier: CA9232620

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12847601T>C , CM000681.2:g.12847601T>C GRCh38
NC_000019.9:g.12958415T>C , CM000681.1:g.12958415T>C GRCh37
NC_000019.8:g.12819415T>C NCBI36
NG_054729.1:g.18671T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000591495.6:c.477-11T>C (MAST1) ENSP00000466470.1:n.477-11T>C
ENST00000699746.1:c.27-11T>C (MAST1) ENSP00000514556.1:n.27-11T>C
ENST00000251472.9:c.489-11T>C (MAST1) MANE Select ENSP00000251472.3:n.489-11T>C
ENST00000251472.8:c.489-11T>C (MAST1) ENSP00000251472.3:n.489-11T>C
ENST00000588379.5:c.349-11T>C (MAST1)
ENST00000589765.1:n.33-21101A>G (HOOK2)
ENST00000590883.1:n.510-11T>C (MAST1)
ENST00000591495.5:c.477-11T>C (MAST1) ENSP00000466470.1:n.477-11T>C
ENST00000592713.1:n.217-11T>C (MAST1)
NM_014975.2:c.489-11T>C (MAST1) NP_055790.1:n.489-11T>C
XM_011527805.1:c.477-11T>C (MAST1) XP_011526107.1:n.477-11T>C
XM_011527806.1:c.201-11T>C (MAST1) XP_011526108.1:n.201-11T>C
XM_011527807.1:c.-40-11T>C (MAST1) XP_011526109.1:n.-40-11T>C
XM_011527805.2:c.477-11T>C (MAST1) XP_011526107.1:n.477-11T>C
NM_014975.3:c.489-11T>C (MAST1) MANE Select NP_055790.1:n.489-11T>C