Canonical Allele Identifier: CA406802626

Gene: TRPM4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49188641G>C , CM000681.2:g.49188641G>C	GRCh38
NC_000019.9:g.49691898G>C , CM000681.1:g.49691898G>C	GRCh37
NC_000019.8:g.54383710G>C	NCBI36
NG_027551.1:g.35883G>C
NG_027551.2:g.35883G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_017636.4:c.1744G>C MANE Select	NP_060106.2:p.Gly582Arg
ENST00000252826.10:c.1744G>C MANE Select	ENSP00000252826.4:p.Gly582Arg
NM_001195227.1:c.1744G>C	NP_001182156.1:p.Gly582Arg
NM_001195227.2:c.1744G>C	NP_001182156.1:p.Gly582Arg
NM_001321281.1:c.1399G>C	NP_001308210.1:p.Gly467Arg
NM_001321281.2:c.1399G>C	NP_001308210.1:p.Gly467Arg
NM_001321282.1:c.136G>C	NP_001308211.1:p.Gly46Arg
NM_001321282.2:c.136G>C	NP_001308211.1:p.Gly46Arg
NM_001321283.1:c.1222G>C	NP_001308212.1:p.Gly408Arg
NM_001321283.2:c.1222G>C	NP_001308212.1:p.Gly408Arg
NM_001321285.1:c.682G>C	NP_001308214.1:p.Gly228Arg
NM_001321285.2:c.682G>C	NP_001308214.1:p.Gly228Arg
NM_017636.3:c.1744G>C	NP_060106.2:p.Gly582Arg
ENST00000252826.9:c.1744G>C	ENSP00000252826.4:p.Gly582Arg
ENST00000427978.6:c.1744G>C	ENSP00000407492.1:p.Gly582Arg
ENST00000595071.5:n.533G>C
ENST00000595519.5:c.*1154G>C	ENSP00000469893.1:n.*1154G>C
ENST00000596338.5:n.1666G>C
ENST00000598502.5:c.*857G>C	ENSP00000470229.1:n.*857G>C
ENST00000598697.5:c.*699G>C	ENSP00000468989.1:n.*699G>C
XM_005259017.1:c.457G>C	XP_005259074.1:p.Gly153Arg
XM_005259018.2:c.136G>C	XP_005259075.1:p.Gly46Arg
XM_011527046.1:c.1222G>C	XP_011525348.1:p.Gly408Arg
XM_024451557.1:c.-406G>C	XP_024307325.1:n.-406G>C