Canonical Allele Identifier: CA2340267840
Gene: TRPM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49157885G= , CM000681.2:g.49157885G= GRCh38
NC_000019.9:g.49661142G= , CM000681.1:g.49661142G= GRCh37
NC_000019.8:g.54352954G= NCBI36
NG_027551.1:g.5127G=
NG_027551.2:g.5127G=

Transcript Alleles

HGVS Amino-acid change
ENST00000252826.10:c.19G= MANE Select ENSP00000252826.4:p.Glu7=
ENST00000252826.9:c.19G= ENSP00000252826.4:p.Glu7=
ENST00000427978.6:c.19G= ENSP00000407492.1:p.Glu7=
ENST00000595519.5:c.19G= ENSP00000469893.1:p.Glu7=
ENST00000596338.5:n.54G=
ENST00000598502.5:c.19G= ENSP00000470229.1:p.Glu7=
ENST00000598691.5:c.19G= ENSP00000473231.1:p.Glu7=
ENST00000598697.5:c.19G= ENSP00000468989.1:p.Glu7=
ENST00000599628.5:c.19G= ENSP00000483753.1:p.Glu7=
NM_001195227.1:c.19G= NP_001182156.1:p.Glu7=
NM_017636.3:c.19G= NP_060106.2:p.Glu7=
XM_011527046.1:c.-148G= XP_011525348.1:n.-148G=
NM_001321281.1:c.19G= NP_001308210.1:p.Glu7=
NM_001321282.1:c.-1354G= NP_001308211.1:n.-1354G=
NM_001321283.1:c.-148G= NP_001308212.1:n.-148G=
NM_001321285.1:c.-311G= NP_001308214.1:n.-311G=
NM_017636.4:c.19G= MANE Select NP_060106.2:p.Glu7=
NM_001195227.2:c.19G= NP_001182156.1:p.Glu7=
NM_001321281.2:c.19G= NP_001308210.1:p.Glu7=
NM_001321282.2:c.-1354G= NP_001308211.1:n.-1354G=
NM_001321283.2:c.-148G= NP_001308212.1:n.-148G=
NM_001321285.2:c.-311G= NP_001308214.1:n.-311G=