Canonical Allele Identifier: CA3287445
Gene: MAST4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.66759828G>A , CM000667.2:g.66759828G>A GRCh38
NC_000005.9:g.66055656G>A , CM000667.1:g.66055656G>A GRCh37
NC_000005.8:g.66091412G>A NCBI36
NG_034036.1:g.168481G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000403625.7:c.483G>A MANE Select ENSP00000385727.1:p.Gln161=
ENST00000403625.6:c.483G>A ENSP00000385727.1:p.Gln161=
ENST00000406039.5:c.483G>A ENSP00000384547.1:p.Gln161=
ENST00000406374.5:c.483G>A ENSP00000385088.1:p.Gln161=
ENST00000432817.5:c.99G>A ENSP00000413573.1:p.Gln33=
ENST00000452953.5:c.101G>A
ENST00000478569.1:n.347G>A
NM_001164664.1:c.483G>A NP_001158136.1:p.Gln161=
NM_001290228.1:c.483G>A NP_001277157.1:p.Gln161=
NM_198828.2:c.483G>A NP_942123.1:p.Gln161=
XM_011543381.1:c.483G>A XP_011541683.1:p.Gln161=
XM_011543382.1:c.483G>A XP_011541684.1:p.Gln161=
XM_011543383.1:c.483G>A XP_011541685.1:p.Gln161=
XM_024446044.1:c.483G>A XP_024301812.1:p.Gln161=
NM_001164664.2:c.483G>A MANE Select NP_001158136.1:p.Gln161=
NM_001290228.2:c.483G>A NP_001277157.1:p.Gln161=
NM_198828.3:c.483G>A NP_942123.1:p.Gln161=
NM_001393524.1:c.483G>A NP_001380453.1:p.Gln161=
NM_001393525.1:c.483G>A NP_001380454.1:p.Gln161=