Canonical Allele Identifier: CA15230999

Gene: TRPC1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142727363A>C , CM000665.2:g.142727363A>C	GRCh38
NC_000003.11:g.142446205A>C , CM000665.1:g.142446205A>C	GRCh37
NC_000003.10:g.143928895A>C	NCBI36
NG_030369.1:g.7940A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698238.1:c.481+2632A>C	ENSP00000513620.1:n.481+2632A>C
ENST00000476941.6:c.172+2632A>C MANE Select	ENSP00000419313.1:n.172+2632A>C
ENST00000273482.10:c.172+2632A>C	ENSP00000273482.6:n.172+2632A>C
ENST00000460401.1:c.167+2632A>C
ENST00000476941.5:c.172+2632A>C	ENSP00000419313.1:n.172+2632A>C
ENST00000612385.1:c.172+2632A>C	ENSP00000481537.1:n.172+2632A>C
NM_001251845.1:c.172+2632A>C	NP_001238774.1:n.172+2632A>C
NM_003304.4:c.172+2632A>C	NP_003295.1:n.172+2632A>C
XM_005247738.2:c.33+2632A>C	XP_005247795.1:n.33+2632A>C
XM_005247739.1:c.33+2632A>C	XP_005247796.1:n.33+2632A>C
XR_241506.2:n.700+2632A>C
XR_924164.1:n.700+2632A>C
XR_924165.1:n.700+2632A>C
XR_924166.1:n.700+2632A>C
XM_005247738.4:c.33+2632A>C	XP_005247795.1:n.33+2632A>C
XM_005247739.2:c.33+2632A>C	XP_005247796.1:n.33+2632A>C
XR_241506.4:n.223+2632A>C
NM_001251845.2:c.172+2632A>C MANE Select	NP_001238774.1:n.172+2632A>C
NM_003304.5:c.172+2632A>C	NP_003295.1:n.172+2632A>C