Canonical Allele Identifier: CA2651762

Gene: TRPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142792921G>A , CM000665.2:g.142792921G>A	GRCh38
NC_000003.11:g.142511763G>A , CM000665.1:g.142511763G>A	GRCh37
NC_000003.10:g.143994453G>A	NCBI36
NG_030369.1:g.73498G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698238.1:c.1844G>A	ENSP00000513620.1:p.Arg615His
ENST00000476941.6:c.1535G>A MANE Select	ENSP00000419313.1:p.Arg512His
ENST00000273482.10:c.1433G>A	ENSP00000273482.6:p.Arg478His
ENST00000476941.5:c.1535G>A	ENSP00000419313.1:p.Arg512His
ENST00000612385.1:c.1433G>A	ENSP00000481537.1:p.Arg478His
NM_001251845.1:c.1535G>A	NP_001238774.1:p.Arg512His
NM_003304.4:c.1433G>A	NP_003295.1:p.Arg478His
XM_005247738.2:c.1241G>A	XP_005247795.1:p.Arg414His
XM_005247739.1:c.1139G>A	XP_005247796.1:p.Arg380His
XR_241506.2:n.1825+7881G>A
XR_924164.1:n.2063G>A
XR_924165.1:n.2063G>A
XR_924166.1:n.2063G>A
XM_005247738.4:c.1241G>A	XP_005247795.1:p.Arg414His
XM_005247739.2:c.1139G>A	XP_005247796.1:p.Arg380His
XM_017007121.2:c.1352G>A	XP_016862610.1:p.Arg451His
XR_001740246.1:n.2194G>A
XR_241506.4:n.1348+7881G>A
NM_001251845.2:c.1535G>A MANE Select	NP_001238774.1:p.Arg512His
NM_003304.5:c.1433G>A	NP_003295.1:p.Arg478His