Canonical Allele Identifier: CA406787736

Gene: TRPM4

Linked Data

• MyVariant Identifiers: chr19:g.49661147G>T (hg19) ; chr19:g.49157890G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49157890G>T , CM000681.2:g.49157890G>T	GRCh38
NC_000019.9:g.49661147G>T , CM000681.1:g.49661147G>T	GRCh37
NC_000019.8:g.54352959G>T	NCBI36
NG_027551.1:g.5132G>T
NG_027551.2:g.5132G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252826.10:c.24G>T MANE Select	ENSP00000252826.4:p.Gln8His
ENST00000252826.9:c.24G>T	ENSP00000252826.4:p.Gln8His
ENST00000427978.6:c.24G>T	ENSP00000407492.1:p.Gln8His
ENST00000595519.5:c.24G>T	ENSP00000469893.1:p.Gln8His
ENST00000596338.5:n.59G>T
ENST00000598502.5:c.24G>T	ENSP00000470229.1:p.Gln8His
ENST00000598691.5:c.24G>T	ENSP00000473231.1:p.Gln8His
ENST00000598697.5:c.24G>T	ENSP00000468989.1:p.Gln8His
ENST00000599628.5:c.24G>T	ENSP00000483753.1:p.Gln8His
NM_001195227.1:c.24G>T	NP_001182156.1:p.Gln8His
NM_017636.3:c.24G>T	NP_060106.2:p.Gln8His
XM_011527046.1:c.-143G>T	XP_011525348.1:n.-143G>T
NM_001321281.1:c.24G>T	NP_001308210.1:p.Gln8His
NM_001321282.1:c.-1349G>T	NP_001308211.1:n.-1349G>T
NM_001321283.1:c.-143G>T	NP_001308212.1:n.-143G>T
NM_001321285.1:c.-306G>T	NP_001308214.1:n.-306G>T
NM_017636.4:c.24G>T MANE Select	NP_060106.2:p.Gln8His
NM_001195227.2:c.24G>T	NP_001182156.1:p.Gln8His
NM_001321281.2:c.24G>T	NP_001308210.1:p.Gln8His
NM_001321282.2:c.-1349G>T	NP_001308211.1:n.-1349G>T
NM_001321283.2:c.-143G>T	NP_001308212.1:n.-143G>T
NM_001321285.2:c.-306G>T	NP_001308214.1:n.-306G>T