Canonical Allele Identifier: CA2651825

Gene: TRPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142803982T>C , CM000665.2:g.142803982T>C	GRCh38
NC_000003.11:g.142522824T>C , CM000665.1:g.142522824T>C	GRCh37
NC_000003.10:g.144005514T>C	NCBI36
NG_030369.1:g.84559T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001251845.2:c.1763T>C MANE Select	NP_001238774.1:p.Ile588Thr
ENST00000476941.6:c.1763T>C MANE Select	ENSP00000419313.1:p.Ile588Thr
NM_001251845.1:c.1763T>C	NP_001238774.1:p.Ile588Thr
NM_003304.4:c.1661T>C	NP_003295.1:p.Ile554Thr
NM_003304.5:c.1661T>C	NP_003295.1:p.Ile554Thr
ENST00000273482.10:c.1661T>C	ENSP00000273482.6:p.Ile554Thr
ENST00000476941.5:c.1763T>C	ENSP00000419313.1:p.Ile588Thr
ENST00000612385.1:c.1661T>C	ENSP00000481537.1:p.Ile554Thr
ENST00000698238.1:c.2072T>C	ENSP00000513620.1:p.Ile691Thr
XM_005247738.2:c.1469T>C	XP_005247795.1:p.Ile490Thr
XM_005247738.4:c.1469T>C	XP_005247795.1:p.Ile490Thr
XM_005247739.1:c.1367T>C	XP_005247796.1:p.Ile456Thr
XM_005247739.2:c.1367T>C	XP_005247796.1:p.Ile456Thr
XM_017007121.2:c.1580T>C	XP_016862610.1:p.Ile527Thr
XR_001740246.1:n.2598T>C
XR_241506.2:n.2007T>C
XR_241506.4:n.1530T>C
XR_924166.1:n.2346T>C