Canonical Allele Identifier: CA1995885128
Gene: TRPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101453062C= , CM000673.2:g.101453062C= GRCh38
NC_000011.9:g.101323793C= , CM000673.1:g.101323793C= GRCh37
NC_000011.8:g.100829003C= NCBI36
NG_011476.1:g.135867G=
NG_011476.2:g.135867G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344327.8:c.2689G= MANE Select ENSP00000340913.3:p.Glu897=
ENST00000344327.7:c.2689G= ENSP00000340913.3:p.Glu897=
ENST00000348423.8:c.2341G= ENSP00000343672.4:p.Glu781=
ENST00000360497.4:c.2524G= ENSP00000353687.4:p.Glu842=
ENST00000532133.5:c.2455G= ENSP00000435574.1:p.Glu819=
NM_004621.5:c.2689G= NP_004612.2:p.Glu897=
XM_006718898.2:c.2614G= XP_006718961.1:p.Glu872=
XM_011542968.1:c.2524G= XP_011541270.1:p.Glu842=
XM_011542968.3:c.2524G= XP_011541270.1:p.Glu842=
XM_017018221.2:c.2341G= XP_016873710.1:p.Glu781=
XR_001747948.2:n.3046G=
NM_004621.6:c.2689G= MANE Select NP_004612.2:p.Glu897=