Canonical Allele Identifier: CA84768826

Gene: TRPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142780938C>G , CM000665.2:g.142780938C>G	GRCh38
NC_000003.11:g.142499780C>G , CM000665.1:g.142499780C>G	GRCh37
NC_000003.10:g.143982470C>G	NCBI36
NG_030369.1:g.61515C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698238.1:c.1178C>G	ENSP00000513620.1:p.Ser393Cys
ENST00000476941.6:c.869C>G MANE Select	ENSP00000419313.1:p.Ser290Cys
ENST00000273482.10:c.767C>G	ENSP00000273482.6:p.Ser256Cys
ENST00000476941.5:c.869C>G	ENSP00000419313.1:p.Ser290Cys
ENST00000612385.1:c.767C>G	ENSP00000481537.1:p.Ser256Cys
NM_001251845.1:c.869C>G	NP_001238774.1:p.Ser290Cys
NM_003304.4:c.767C>G	NP_003295.1:p.Ser256Cys
XM_005247738.2:c.575C>G	XP_005247795.1:p.Ser192Cys
XM_005247739.1:c.473C>G	XP_005247796.1:p.Ser158Cys
XR_241506.2:n.1397C>G
XR_924164.1:n.1397C>G
XR_924165.1:n.1397C>G
XR_924166.1:n.1397C>G
XM_005247738.4:c.575C>G	XP_005247795.1:p.Ser192Cys
XM_005247739.2:c.473C>G	XP_005247796.1:p.Ser158Cys
XM_017007121.2:c.686C>G	XP_016862610.1:p.Ser229Cys
XR_001740246.1:n.1528C>G
XR_241506.4:n.920C>G
NM_001251845.2:c.869C>G MANE Select	NP_001238774.1:p.Ser290Cys
NM_003304.5:c.767C>G	NP_003295.1:p.Ser256Cys