Canonical Allele Identifier: CA2340267841
Gene: TRPM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49157886_49157887delinsAG , CM000681.2:g.49157886_49157887delinsAG GRCh38
NC_000019.9:g.49661143_49661144delinsAG , CM000681.1:g.49661143_49661144delinsAG GRCh37
NC_000019.8:g.54352955_54352956delinsAG NCBI36
NG_027551.1:g.5128_5129delinsAG
NG_027551.2:g.5128_5129delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000252826.10:c.20_21delinsAG MANE Select ENSP00000252826.4:p.Glu7=
ENST00000252826.9:c.20_21delinsAG ENSP00000252826.4:p.Glu7=
ENST00000427978.6:c.20_21delinsAG ENSP00000407492.1:p.Glu7=
ENST00000595519.5:c.20_21delinsAG ENSP00000469893.1:p.Glu7=
ENST00000596338.5:n.55_56delinsAG
ENST00000598502.5:c.20_21delinsAG ENSP00000470229.1:p.Glu7=
ENST00000598691.5:c.20_21delinsAG ENSP00000473231.1:p.Glu7=
ENST00000598697.5:c.20_21delinsAG ENSP00000468989.1:p.Glu7=
ENST00000599628.5:c.20_21delinsAG ENSP00000483753.1:p.Glu7=
NM_001195227.1:c.20_21delinsAG NP_001182156.1:p.Glu7=
NM_017636.3:c.20_21delinsAG NP_060106.2:p.Glu7=
XM_011527046.1:c.-147_-146delinsAG XP_011525348.1:n.-147_-146delinsAG
NM_001321281.1:c.20_21delinsAG NP_001308210.1:p.Glu7=
NM_001321282.1:c.-1353_-1352delinsAG NP_001308211.1:n.-1353_-1352delinsAG
NM_001321283.1:c.-147_-146delinsAG NP_001308212.1:n.-147_-146delinsAG
NM_001321285.1:c.-310_-309delinsAG NP_001308214.1:n.-310_-309delinsAG
NM_017636.4:c.20_21delinsAG MANE Select NP_060106.2:p.Glu7=
NM_001195227.2:c.20_21delinsAG NP_001182156.1:p.Glu7=
NM_001321281.2:c.20_21delinsAG NP_001308210.1:p.Glu7=
NM_001321282.2:c.-1353_-1352delinsAG NP_001308211.1:n.-1353_-1352delinsAG
NM_001321283.2:c.-147_-146delinsAG NP_001308212.1:n.-147_-146delinsAG
NM_001321285.2:c.-310_-309delinsAG NP_001308214.1:n.-310_-309delinsAG