Canonical Allele Identifier: CA2615685740

Gene: TRPC6

Linked Data

• gnomAD v4: 11-101482935-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101482935A>T , CM000673.2:g.101482935A>T	GRCh38
NC_000011.9:g.101353666A>T , CM000673.1:g.101353666A>T	GRCh37
NC_000011.8:g.100858876A>T	NCBI36
NG_011476.1:g.105994T>A
NG_011476.2:g.105994T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000344327.8:c.1510+14T>A MANE Select	ENSP00000340913.3:n.1510+14T>A
ENST00000344327.7:c.1510+14T>A	ENSP00000340913.3:n.1510+14T>A
ENST00000348423.8:c.1162+14T>A	ENSP00000343672.4:n.1162+14T>A
ENST00000360497.4:c.1345+14T>A	ENSP00000353687.4:n.1345+14T>A
ENST00000532133.5:c.1510+14T>A	ENSP00000435574.1:n.1510+14T>A
NM_004621.5:c.1510+14T>A	NP_004612.2:n.1510+14T>A
XM_006718898.2:c.1510+14T>A	XP_006718961.1:n.1510+14T>A
XM_011542968.1:c.1345+14T>A	XP_011541270.1:n.1345+14T>A
XM_011542969.1:c.1510+14T>A	XP_011541271.1:n.1510+14T>A
XM_011542968.3:c.1345+14T>A	XP_011541270.1:n.1345+14T>A
XM_017018221.2:c.1162+14T>A	XP_016873710.1:n.1162+14T>A
XR_001747948.2:n.1866+14T>A
NM_004621.6:c.1510+14T>A MANE Select	NP_004612.2:n.1510+14T>A