Canonical Allele Identifier: CA406787648

Gene: TRPM4

Linked Data

• dbSNP Id: rs1600378229
• gnomAD v3: 19-49157874-T-G
• gnomAD v4: 19-49157874-T-G
• MyVariant Identifiers: chr19:g.49661131T>G (hg19) ; chr19:g.49157874T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49157874T>G , CM000681.2:g.49157874T>G	GRCh38
NC_000019.9:g.49661131T>G , CM000681.1:g.49661131T>G	GRCh37
NC_000019.8:g.54352943T>G	NCBI36
NG_027551.1:g.5116T>G
NG_027551.2:g.5116T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252826.10:c.8T>G MANE Select	ENSP00000252826.4:p.Val3Gly
ENST00000252826.9:c.8T>G	ENSP00000252826.4:p.Val3Gly
ENST00000427978.6:c.8T>G	ENSP00000407492.1:p.Val3Gly
ENST00000595519.5:c.8T>G	ENSP00000469893.1:p.Val3Gly
ENST00000596338.5:n.43T>G
ENST00000598502.5:c.8T>G	ENSP00000470229.1:p.Val3Gly
ENST00000598691.5:c.8T>G	ENSP00000473231.1:p.Val3Gly
ENST00000598697.5:c.8T>G	ENSP00000468989.1:p.Val3Gly
ENST00000599628.5:c.8T>G	ENSP00000483753.1:p.Val3Gly
NM_001195227.1:c.8T>G	NP_001182156.1:p.Val3Gly
NM_017636.3:c.8T>G	NP_060106.2:p.Val3Gly
XM_011527046.1:c.-159T>G	XP_011525348.1:n.-159T>G
NM_001321281.1:c.8T>G	NP_001308210.1:p.Val3Gly
NM_001321282.1:c.-1365T>G	NP_001308211.1:n.-1365T>G
NM_001321283.1:c.-159T>G	NP_001308212.1:n.-159T>G
NM_001321285.1:c.-322T>G	NP_001308214.1:n.-322T>G
NM_017636.4:c.8T>G MANE Select	NP_060106.2:p.Val3Gly
NM_001195227.2:c.8T>G	NP_001182156.1:p.Val3Gly
NM_001321281.2:c.8T>G	NP_001308210.1:p.Val3Gly
NM_001321282.2:c.-1365T>G	NP_001308211.1:n.-1365T>G
NM_001321283.2:c.-159T>G	NP_001308212.1:n.-159T>G
NM_001321285.2:c.-322T>G	NP_001308214.1:n.-322T>G