Canonical Allele Identifier: CA406787719

Gene: TRPM4

Linked Data

• gnomAD v4: 19-49157887-G-T
• MyVariant Identifiers: chr19:g.49661144G>T (hg19) ; chr19:g.49157887G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49157887G>T , CM000681.2:g.49157887G>T	GRCh38
NC_000019.9:g.49661144G>T , CM000681.1:g.49661144G>T	GRCh37
NC_000019.8:g.54352956G>T	NCBI36
NG_027551.1:g.5129G>T
NG_027551.2:g.5129G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252826.10:c.21G>T MANE Select	ENSP00000252826.4:p.Glu7Asp
ENST00000252826.9:c.21G>T	ENSP00000252826.4:p.Glu7Asp
ENST00000427978.6:c.21G>T	ENSP00000407492.1:p.Glu7Asp
ENST00000595519.5:c.21G>T	ENSP00000469893.1:p.Glu7Asp
ENST00000596338.5:n.56G>T
ENST00000598502.5:c.21G>T	ENSP00000470229.1:p.Glu7Asp
ENST00000598691.5:c.21G>T	ENSP00000473231.1:p.Glu7Asp
ENST00000598697.5:c.21G>T	ENSP00000468989.1:p.Glu7Asp
ENST00000599628.5:c.21G>T	ENSP00000483753.1:p.Glu7Asp
NM_001195227.1:c.21G>T	NP_001182156.1:p.Glu7Asp
NM_017636.3:c.21G>T	NP_060106.2:p.Glu7Asp
XM_011527046.1:c.-146G>T	XP_011525348.1:n.-146G>T
NM_001321281.1:c.21G>T	NP_001308210.1:p.Glu7Asp
NM_001321282.1:c.-1352G>T	NP_001308211.1:n.-1352G>T
NM_001321283.1:c.-146G>T	NP_001308212.1:n.-146G>T
NM_001321285.1:c.-309G>T	NP_001308214.1:n.-309G>T
NM_017636.4:c.21G>T MANE Select	NP_060106.2:p.Glu7Asp
NM_001195227.2:c.21G>T	NP_001182156.1:p.Glu7Asp
NM_001321281.2:c.21G>T	NP_001308210.1:p.Glu7Asp
NM_001321282.2:c.-1352G>T	NP_001308211.1:n.-1352G>T
NM_001321283.2:c.-146G>T	NP_001308212.1:n.-146G>T
NM_001321285.2:c.-309G>T	NP_001308214.1:n.-309G>T