Canonical Allele Identifier: CA2651589
Gene: TRPC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142748333C>T , CM000665.2:g.142748333C>T GRCh38
NC_000003.11:g.142467175C>T , CM000665.1:g.142467175C>T GRCh37
NC_000003.10:g.143949865C>T NCBI36
NG_030369.1:g.28910C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698238.1:c.814C>T ENSP00000513620.1:p.Arg272Cys
ENST00000476941.6:c.505C>T MANE Select ENSP00000419313.1:p.Arg169Cys
ENST00000273482.10:c.403C>T ENSP00000273482.6:p.Arg135Cys
ENST00000460401.1:c.243C>T
ENST00000476941.5:c.505C>T ENSP00000419313.1:p.Arg169Cys
ENST00000612385.1:c.403C>T ENSP00000481537.1:p.Arg135Cys
NM_001251845.1:c.505C>T NP_001238774.1:p.Arg169Cys
NM_003304.4:c.403C>T NP_003295.1:p.Arg135Cys
XM_005247738.2:c.211C>T XP_005247795.1:p.Arg71Cys
XM_005247739.1:c.109C>T XP_005247796.1:p.Arg37Cys
XR_241506.2:n.1033C>T
XR_924164.1:n.1033C>T
XR_924165.1:n.1033C>T
XR_924166.1:n.1033C>T
XM_005247738.4:c.211C>T XP_005247795.1:p.Arg71Cys
XM_005247739.2:c.109C>T XP_005247796.1:p.Arg37Cys
XM_017007121.2:c.322C>T XP_016862610.1:p.Arg108Cys
XR_001740246.1:n.1164C>T
XR_241506.4:n.556C>T
NM_001251845.2:c.505C>T MANE Select NP_001238774.1:p.Arg169Cys
NM_003304.5:c.403C>T NP_003295.1:p.Arg135Cys