Canonical Allele Identifier: CA382441594

Gene: TRPC6

Linked Data

• dbSNP Id: rs1419291323
• gnomAD v2: 11-101353763-C-T
• gnomAD v4: 11-101483032-C-T
• MyVariant Identifiers: chr11:g.101353763C>T (hg19) ; chr11:g.101483032C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101483032C>T , CM000673.2:g.101483032C>T	GRCh38
NC_000011.9:g.101353763C>T , CM000673.1:g.101353763C>T	GRCh37
NC_000011.8:g.100858973C>T	NCBI36
NG_011476.1:g.105897G>A
NG_011476.2:g.105897G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000344327.8:c.1427G>A MANE Select	ENSP00000340913.3:p.Ser476Asn
ENST00000344327.7:c.1427G>A	ENSP00000340913.3:p.Ser476Asn
ENST00000348423.8:c.1079G>A	ENSP00000343672.4:p.Ser360Asn
ENST00000360497.4:c.1262G>A	ENSP00000353687.4:p.Ser421Asn
ENST00000532133.5:c.1427G>A	ENSP00000435574.1:p.Ser476Asn
NM_004621.5:c.1427G>A	NP_004612.2:p.Ser476Asn
XM_006718898.2:c.1427G>A	XP_006718961.1:p.Ser476Asn
XM_011542968.1:c.1262G>A	XP_011541270.1:p.Ser421Asn
XM_011542969.1:c.1427G>A	XP_011541271.1:p.Ser476Asn
XM_011542968.3:c.1262G>A	XP_011541270.1:p.Ser421Asn
XM_017018221.2:c.1079G>A	XP_016873710.1:p.Ser360Asn
XR_001747948.2:n.1783G>A
NM_004621.6:c.1427G>A MANE Select	NP_004612.2:p.Ser476Asn