Canonical Allele Identifier: CA1995885652
Gene: TRPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101453528T= , CM000673.2:g.101453528T= GRCh38
NC_000011.9:g.101324259T= , CM000673.1:g.101324259T= GRCh37
NC_000011.8:g.100829469T= NCBI36
NG_011476.1:g.135401A=
NG_011476.2:g.135401A=

Transcript Alleles

HGVS Amino-acid change
ENST00000344327.8:c.2644+122A= MANE Select ENSP00000340913.3:n.2644+122A=
ENST00000344327.7:c.2644+122A= ENSP00000340913.3:n.2644+122A=
ENST00000348423.8:c.2296+122A= ENSP00000343672.4:n.2296+122A=
ENST00000360497.4:c.2479+122A= ENSP00000353687.4:n.2479+122A=
ENST00000532133.5:c.2410+122A= ENSP00000435574.1:n.2410+122A=
NM_004621.5:c.2644+122A= NP_004612.2:n.2644+122A=
XM_006718898.2:c.2569+122A= XP_006718961.1:n.2569+122A=
XM_011542968.1:c.2479+122A= XP_011541270.1:n.2479+122A=
XM_011542968.3:c.2479+122A= XP_011541270.1:n.2479+122A=
XM_017018221.2:c.2296+122A= XP_016873710.1:n.2296+122A=
XR_001747948.2:n.3001+122A=
NM_004621.6:c.2644+122A= MANE Select NP_004612.2:n.2644+122A=