Canonical Allele Identifier: CA382487034
Gene: TRPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101453083C>T , CM000673.2:g.101453083C>T GRCh38
NC_000011.9:g.101323814C>T , CM000673.1:g.101323814C>T GRCh37
NC_000011.8:g.100829024C>T NCBI36
NG_011476.1:g.135846G>A
NG_011476.2:g.135846G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344327.8:c.2668G>A MANE Select ENSP00000340913.3:p.Asp890Asn
ENST00000344327.7:c.2668G>A ENSP00000340913.3:p.Asp890Asn
ENST00000348423.8:c.2320G>A ENSP00000343672.4:p.Asp774Asn
ENST00000360497.4:c.2503G>A ENSP00000353687.4:p.Asp835Asn
ENST00000532133.5:c.2434G>A ENSP00000435574.1:p.Asp812Asn
NM_004621.5:c.2668G>A NP_004612.2:p.Asp890Asn
XM_006718898.2:c.2593G>A XP_006718961.1:p.Asp865Asn
XM_011542968.1:c.2503G>A XP_011541270.1:p.Asp835Asn
XM_011542968.3:c.2503G>A XP_011541270.1:p.Asp835Asn
XM_017018221.2:c.2320G>A XP_016873710.1:p.Asp774Asn
XR_001747948.2:n.3025G>A
NM_004621.6:c.2668G>A MANE Select NP_004612.2:p.Asp890Asn