Canonical Allele Identifier: CA2651489

Gene: TRPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142724623T>C , CM000665.2:g.142724623T>C	GRCh38
NC_000003.11:g.142443465T>C , CM000665.1:g.142443465T>C	GRCh37
NC_000003.10:g.143926155T>C	NCBI36
NG_030369.1:g.5200T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698238.1:c.373T>C	ENSP00000513620.1:p.Ser125Pro
ENST00000476941.6:c.64T>C MANE Select	ENSP00000419313.1:p.Ser22Pro
ENST00000273482.10:c.64T>C	ENSP00000273482.6:p.Ser22Pro
ENST00000460401.1:c.59T>C
ENST00000476941.5:c.64T>C	ENSP00000419313.1:p.Ser22Pro
ENST00000612385.1:c.64T>C	ENSP00000481537.1:p.Ser22Pro
NM_001251845.1:c.64T>C	NP_001238774.1:p.Ser22Pro
NM_003304.4:c.64T>C	NP_003295.1:p.Ser22Pro
XM_005247738.2:c.-76T>C	XP_005247795.1:n.-76T>C
XM_005247739.1:c.-76T>C	XP_005247796.1:n.-76T>C
XR_241506.2:n.592T>C
XR_924164.1:n.592T>C
XR_924165.1:n.592T>C
XR_924166.1:n.592T>C
XM_005247738.4:c.-76T>C	XP_005247795.1:n.-76T>C
XM_005247739.2:c.-76T>C	XP_005247796.1:n.-76T>C
XR_241506.4:n.115T>C
NM_001251845.2:c.64T>C MANE Select	NP_001238774.1:p.Ser22Pro
NM_003304.5:c.64T>C	NP_003295.1:p.Ser22Pro