Canonical Allele Identifier: CA783408225

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12847594G>T , CM000681.2:g.12847594G>T GRCh38
NC_000019.9:g.12958408G>T , CM000681.1:g.12958408G>T GRCh37
NC_000019.8:g.12819408G>T NCBI36
NG_054729.1:g.18664G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000591495.6:c.477-18G>T (MAST1) ENSP00000466470.1:n.477-18G>T
ENST00000699746.1:c.27-18G>T (MAST1) ENSP00000514556.1:n.27-18G>T
ENST00000251472.9:c.489-18G>T (MAST1) MANE Select ENSP00000251472.3:n.489-18G>T
ENST00000251472.8:c.489-18G>T (MAST1) ENSP00000251472.3:n.489-18G>T
ENST00000588379.5:c.349-18G>T (MAST1)
ENST00000589765.1:n.33-21094C>A (HOOK2)
ENST00000590883.1:n.510-18G>T (MAST1)
ENST00000591495.5:c.477-18G>T (MAST1) ENSP00000466470.1:n.477-18G>T
ENST00000592713.1:n.217-18G>T (MAST1)
NM_014975.2:c.489-18G>T (MAST1) NP_055790.1:n.489-18G>T
XM_011527805.1:c.477-18G>T (MAST1) XP_011526107.1:n.477-18G>T
XM_011527806.1:c.201-18G>T (MAST1) XP_011526108.1:n.201-18G>T
XM_011527807.1:c.-40-18G>T (MAST1) XP_011526109.1:n.-40-18G>T
XM_011527805.2:c.477-18G>T (MAST1) XP_011526107.1:n.477-18G>T
NM_014975.3:c.489-18G>T (MAST1) MANE Select NP_055790.1:n.489-18G>T