Canonical Allele Identifier: CA2651735
Gene: TRPC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142791084C>T , CM000665.2:g.142791084C>T GRCh38
NC_000003.11:g.142509926C>T , CM000665.1:g.142509926C>T GRCh37
NC_000003.10:g.143992616C>T NCBI36
NG_030369.1:g.71661C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698238.1:c.1672C>T ENSP00000513620.1:p.Arg558Cys
ENST00000476941.6:c.1363C>T MANE Select ENSP00000419313.1:p.Arg455Cys
ENST00000273482.10:c.1261C>T ENSP00000273482.6:p.Arg421Cys
ENST00000476941.5:c.1363C>T ENSP00000419313.1:p.Arg455Cys
ENST00000612385.1:c.1261C>T ENSP00000481537.1:p.Arg421Cys
NM_001251845.1:c.1363C>T NP_001238774.1:p.Arg455Cys
NM_003304.4:c.1261C>T NP_003295.1:p.Arg421Cys
XM_005247738.2:c.1069C>T XP_005247795.1:p.Arg357Cys
XM_005247739.1:c.967C>T XP_005247796.1:p.Arg323Cys
XR_241506.2:n.1825+6044C>T
XR_924164.1:n.1891C>T
XR_924165.1:n.1891C>T
XR_924166.1:n.1891C>T
XM_005247738.4:c.1069C>T XP_005247795.1:p.Arg357Cys
XM_005247739.2:c.967C>T XP_005247796.1:p.Arg323Cys
XM_017007121.2:c.1180C>T XP_016862610.1:p.Arg394Cys
XR_001740246.1:n.2022C>T
XR_241506.4:n.1348+6044C>T
NM_001251845.2:c.1363C>T MANE Select NP_001238774.1:p.Arg455Cys
NM_003304.5:c.1261C>T NP_003295.1:p.Arg421Cys