Canonical Allele Identifier: CA354825139

Gene: TRPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142777742G>C , CM000665.2:g.142777742G>C	GRCh38
NC_000003.11:g.142496584G>C , CM000665.1:g.142496584G>C	GRCh37
NC_000003.10:g.143979274G>C	NCBI36
NG_030369.1:g.58319G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698238.1:c.1052G>C	ENSP00000513620.1:p.Ser351Thr
ENST00000476941.6:c.743G>C MANE Select	ENSP00000419313.1:p.Ser248Thr
ENST00000273482.10:c.641G>C	ENSP00000273482.6:p.Ser214Thr
ENST00000476941.5:c.743G>C	ENSP00000419313.1:p.Ser248Thr
ENST00000612385.1:c.641G>C	ENSP00000481537.1:p.Ser214Thr
NM_001251845.1:c.743G>C	NP_001238774.1:p.Ser248Thr
NM_003304.4:c.641G>C	NP_003295.1:p.Ser214Thr
XM_005247738.2:c.449G>C	XP_005247795.1:p.Ser150Thr
XM_005247739.1:c.347G>C	XP_005247796.1:p.Ser116Thr
XR_241506.2:n.1271G>C
XR_924164.1:n.1271G>C
XR_924165.1:n.1271G>C
XR_924166.1:n.1271G>C
XM_005247738.4:c.449G>C	XP_005247795.1:p.Ser150Thr
XM_005247739.2:c.347G>C	XP_005247796.1:p.Ser116Thr
XM_017007121.2:c.560G>C	XP_016862610.1:p.Ser187Thr
XR_001740246.1:n.1402G>C
XR_241506.4:n.794G>C
NM_001251845.2:c.743G>C MANE Select	NP_001238774.1:p.Ser248Thr
NM_003304.5:c.641G>C	NP_003295.1:p.Ser214Thr