Canonical Allele Identifier: CA382441567

Gene: TRPC6

Linked Data

• gnomAD v4: 11-101483026-T-C
• MyVariant Identifiers: chr11:g.101353757T>C (hg19) ; chr11:g.101483026T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101483026T>C , CM000673.2:g.101483026T>C	GRCh38
NC_000011.9:g.101353757T>C , CM000673.1:g.101353757T>C	GRCh37
NC_000011.8:g.100858967T>C	NCBI36
NG_011476.1:g.105903A>G
NG_011476.2:g.105903A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344327.8:c.1433A>G MANE Select	ENSP00000340913.3:p.Asp478Gly
ENST00000344327.7:c.1433A>G	ENSP00000340913.3:p.Asp478Gly
ENST00000348423.8:c.1085A>G	ENSP00000343672.4:p.Asp362Gly
ENST00000360497.4:c.1268A>G	ENSP00000353687.4:p.Asp423Gly
ENST00000532133.5:c.1433A>G	ENSP00000435574.1:p.Asp478Gly
NM_004621.5:c.1433A>G	NP_004612.2:p.Asp478Gly
XM_006718898.2:c.1433A>G	XP_006718961.1:p.Asp478Gly
XM_011542968.1:c.1268A>G	XP_011541270.1:p.Asp423Gly
XM_011542969.1:c.1433A>G	XP_011541271.1:p.Asp478Gly
XM_011542968.3:c.1268A>G	XP_011541270.1:p.Asp423Gly
XM_017018221.2:c.1085A>G	XP_016873710.1:p.Asp362Gly
XR_001747948.2:n.1789A>G
NM_004621.6:c.1433A>G MANE Select	NP_004612.2:p.Asp478Gly