Canonical Allele Identifier: CA2651911

Gene: TRPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142806198G>A , CM000665.2:g.142806198G>A	GRCh38
NC_000003.11:g.142525040G>A , CM000665.1:g.142525040G>A	GRCh37
NC_000003.10:g.144007730G>A	NCBI36
NG_030369.1:g.86775G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698238.1:c.2654G>A	ENSP00000513620.1:p.Arg885Gln
ENST00000476941.6:c.2345G>A MANE Select	ENSP00000419313.1:p.Arg782Gln
ENST00000273482.10:c.2243G>A	ENSP00000273482.6:p.Arg748Gln
ENST00000476941.5:c.2345G>A	ENSP00000419313.1:p.Arg782Gln
ENST00000612385.1:c.2243G>A	ENSP00000481537.1:p.Arg748Gln
NM_001251845.1:c.2345G>A	NP_001238774.1:p.Arg782Gln
NM_003304.4:c.2243G>A	NP_003295.1:p.Arg748Gln
XM_005247738.2:c.2051G>A	XP_005247795.1:p.Arg684Gln
XM_005247739.1:c.1949G>A	XP_005247796.1:p.Arg650Gln
XM_005247738.4:c.2051G>A	XP_005247795.1:p.Arg684Gln
XM_005247739.2:c.1949G>A	XP_005247796.1:p.Arg650Gln
XM_017007121.2:c.2162G>A	XP_016862610.1:p.Arg721Gln
XR_241506.4:n.2112G>A
NM_001251845.2:c.2345G>A MANE Select	NP_001238774.1:p.Arg782Gln
NM_003304.5:c.2243G>A	NP_003295.1:p.Arg748Gln