Canonical Allele Identifier: CA2615684321

Gene: TRPC6

Linked Data

• gnomAD v4: 11-101453537-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101453537C>G , CM000673.2:g.101453537C>G	GRCh38
NC_000011.9:g.101324268C>G , CM000673.1:g.101324268C>G	GRCh37
NC_000011.8:g.100829478C>G	NCBI36
NG_011476.1:g.135392G>C
NG_011476.2:g.135392G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344327.8:c.2644+113G>C MANE Select	ENSP00000340913.3:n.2644+113G>C
ENST00000344327.7:c.2644+113G>C	ENSP00000340913.3:n.2644+113G>C
ENST00000348423.8:c.2296+113G>C	ENSP00000343672.4:n.2296+113G>C
ENST00000360497.4:c.2479+113G>C	ENSP00000353687.4:n.2479+113G>C
ENST00000532133.5:c.2410+113G>C	ENSP00000435574.1:n.2410+113G>C
NM_004621.5:c.2644+113G>C	NP_004612.2:n.2644+113G>C
XM_006718898.2:c.2569+113G>C	XP_006718961.1:n.2569+113G>C
XM_011542968.1:c.2479+113G>C	XP_011541270.1:n.2479+113G>C
XM_011542968.3:c.2479+113G>C	XP_011541270.1:n.2479+113G>C
XM_017018221.2:c.2296+113G>C	XP_016873710.1:n.2296+113G>C
XR_001747948.2:n.3001+113G>C
NM_004621.6:c.2644+113G>C MANE Select	NP_004612.2:n.2644+113G>C