Canonical Allele Identifier: CA12117106
Gene: MAST4 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1697137

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.67156347G>A , CM000667.2:g.67156347G>A GRCh38
NC_000005.8:g.66487931G>A NCBI36
NC_000005.9:g.66452175G>A , CM000667.1:g.66452175G>A GRCh37
NG_034036.1:g.565000G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261569.11:c.3066+2767G>A ENSP00000261569.7:p.=
ENST00000403625.6:c.3648+2767G>A ENSP00000385727.1:p.=
ENST00000403666.5:c.3081+2767G>A ENSP00000384313.1:p.=
ENST00000405643.5:c.3111+2767G>A ENSP00000384099.1:p.=
ENST00000443808.1:n.817+2767G>A
NM_001164664.1:c.3648+2767G>A VV NP_001158136.1:p.=
NM_001290226.1:c.3030+2767G>A VV NP_001277155.1:p.=
NM_001290227.1:c.2865+2767G>A VV NP_001277156.1:p.=
NM_001297651.1:c.3066+2767G>A VV NP_001284580.1:p.=
NM_015183.2:c.3081+2767G>A VV NP_055998.1:p.=
XM_006714606.2:c.3066+2767G>A XP_006714669.1:p.=
XM_006714610.1:c.2865+2767G>A XP_006714673.1:p.=
XM_011543381.1:c.3945+2767G>A XP_011541683.1:p.=
XM_011543382.1:c.3759+2767G>A XP_011541684.1:p.=
XM_011543383.1:c.3684+2767G>A XP_011541685.1:p.=
XM_011543384.1:c.3048+2767G>A XP_011541686.1:p.=
XM_011543385.1:c.3021+2767G>A XP_011541687.1:p.=
XM_011543386.1:c.3012+2767G>A XP_011541688.1:p.=