Canonical Allele Identifier: CA9569642

Gene: TRPM4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49200420C>A , CM000681.2:g.49200420C>A	GRCh38
NC_000019.9:g.49703677C>A , CM000681.1:g.49703677C>A	GRCh37
NC_000019.8:g.54395489C>A	NCBI36
NG_027551.1:g.47662C>A
NG_027551.2:g.47662C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252826.10:c.2766C>A MANE Select	ENSP00000252826.4:p.Ile922=
ENST00000252826.9:c.2766C>A	ENSP00000252826.4:p.Ile922=
ENST00000427978.6:c.2331C>A	ENSP00000407492.1:p.Ile777=
ENST00000595071.5:n.1730C>A
ENST00000595519.5:c.*2176C>A	ENSP00000469893.1:n.*2176C>A
ENST00000596338.5:n.2863C>A
ENST00000598502.5:c.*1879C>A	ENSP00000470229.1:n.*1879C>A
ENST00000598697.5:c.*1721C>A	ENSP00000468989.1:n.*1721C>A
NM_001195227.1:c.2331C>A	NP_001182156.1:p.Ile777=
NM_017636.3:c.2766C>A	NP_060106.2:p.Ile922=
XM_005259017.1:c.1479C>A	XP_005259074.1:p.Ile493=
XM_005259018.2:c.1158C>A	XP_005259075.1:p.Ile386=
XM_011527046.1:c.2244C>A	XP_011525348.1:p.Ile748=
NM_001321281.1:c.2421C>A	NP_001308210.1:p.Ile807=
NM_001321282.1:c.1158C>A	NP_001308211.1:p.Ile386=
NM_001321283.1:c.2244C>A	NP_001308212.1:p.Ile748=
NM_001321285.1:c.1704C>A	NP_001308214.1:p.Ile568=
XM_024451557.1:c.792C>A	XP_024307325.1:p.Ile264=
NM_017636.4:c.2766C>A MANE Select	NP_060106.2:p.Ile922=
NM_001195227.2:c.2331C>A	NP_001182156.1:p.Ile777=
NM_001321281.2:c.2421C>A	NP_001308210.1:p.Ile807=
NM_001321282.2:c.1158C>A	NP_001308211.1:p.Ile386=
NM_001321283.2:c.2244C>A	NP_001308212.1:p.Ile748=
NM_001321285.2:c.1704C>A	NP_001308214.1:p.Ile568=