Canonical Allele Identifier: CA406787725

Gene: TRPM4

Linked Data

• gnomAD v4: 19-49157888-C-T
• MyVariant Identifiers: chr19:g.49661145C>T (hg19) ; chr19:g.49157888C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49157888C>T , CM000681.2:g.49157888C>T	GRCh38
NC_000019.9:g.49661145C>T , CM000681.1:g.49661145C>T	GRCh37
NC_000019.8:g.54352957C>T	NCBI36
NG_027551.1:g.5130C>T
NG_027551.2:g.5130C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252826.10:c.22C>T MANE Select	ENSP00000252826.4:p.Gln8Ter
ENST00000252826.9:c.22C>T	ENSP00000252826.4:p.Gln8Ter
ENST00000427978.6:c.22C>T	ENSP00000407492.1:p.Gln8Ter
ENST00000595519.5:c.22C>T	ENSP00000469893.1:p.Gln8Ter
ENST00000596338.5:n.57C>T
ENST00000598502.5:c.22C>T	ENSP00000470229.1:p.Gln8Ter
ENST00000598691.5:c.22C>T	ENSP00000473231.1:p.Gln8Ter
ENST00000598697.5:c.22C>T	ENSP00000468989.1:p.Gln8Ter
ENST00000599628.5:c.22C>T	ENSP00000483753.1:p.Gln8Ter
NM_001195227.1:c.22C>T	NP_001182156.1:p.Gln8Ter
NM_017636.3:c.22C>T	NP_060106.2:p.Gln8Ter
XM_011527046.1:c.-145C>T	XP_011525348.1:n.-145C>T
NM_001321281.1:c.22C>T	NP_001308210.1:p.Gln8Ter
NM_001321282.1:c.-1351C>T	NP_001308211.1:n.-1351C>T
NM_001321283.1:c.-145C>T	NP_001308212.1:n.-145C>T
NM_001321285.1:c.-308C>T	NP_001308214.1:n.-308C>T
NM_017636.4:c.22C>T MANE Select	NP_060106.2:p.Gln8Ter
NM_001195227.2:c.22C>T	NP_001182156.1:p.Gln8Ter
NM_001321281.2:c.22C>T	NP_001308210.1:p.Gln8Ter
NM_001321282.2:c.-1351C>T	NP_001308211.1:n.-1351C>T
NM_001321283.2:c.-145C>T	NP_001308212.1:n.-145C>T
NM_001321285.2:c.-308C>T	NP_001308214.1:n.-308C>T