Canonical Allele Identifier: CA2651544
Gene: TRPC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142736460G>A , CM000665.2:g.142736460G>A GRCh38
NC_000003.11:g.142455302G>A , CM000665.1:g.142455302G>A GRCh37
NC_000003.10:g.143937992G>A NCBI36
NG_030369.1:g.17037G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698238.1:c.563G>A ENSP00000513620.1:p.Arg188Lys
ENST00000476941.6:c.254G>A MANE Select ENSP00000419313.1:p.Arg85Lys
ENST00000273482.10:c.254G>A ENSP00000273482.6:p.Arg85Lys
ENST00000460401.1:c.167+11729G>A
ENST00000476941.5:c.254G>A ENSP00000419313.1:p.Arg85Lys
ENST00000612385.1:c.254G>A ENSP00000481537.1:p.Arg85Lys
NM_001251845.1:c.254G>A NP_001238774.1:p.Arg85Lys
NM_003304.4:c.254G>A NP_003295.1:p.Arg85Lys
XM_005247738.2:c.34-7025G>A XP_005247795.1:n.34-7025G>A
XM_005247739.1:c.33+11729G>A XP_005247796.1:n.33+11729G>A
XR_241506.2:n.782G>A
XR_924164.1:n.782G>A
XR_924165.1:n.782G>A
XR_924166.1:n.782G>A
XM_005247738.4:c.34-7025G>A XP_005247795.1:n.34-7025G>A
XM_005247739.2:c.33+11729G>A XP_005247796.1:n.33+11729G>A
XM_017007121.2:c.71G>A XP_016862610.1:p.Arg24Lys
XR_001740246.1:n.1015G>A
XR_241506.4:n.305G>A
NM_001251845.2:c.254G>A MANE Select NP_001238774.1:p.Arg85Lys
NM_003304.5:c.254G>A NP_003295.1:p.Arg85Lys