Canonical Allele Identifier: CA1995899049
Gene: TRPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101472363A= , CM000673.2:g.101472363A= GRCh38
NC_000011.9:g.101343094A= , CM000673.1:g.101343094A= GRCh37
NC_000011.8:g.100848304A= NCBI36
NG_011476.1:g.116566T=
NG_011476.2:g.116566T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344327.8:c.2010-31T= MANE Select ENSP00000340913.3:n.2010-31T=
ENST00000344327.7:c.2010-31T= ENSP00000340913.3:n.2010-31T=
ENST00000348423.8:c.1662-31T= ENSP00000343672.4:n.1662-31T=
ENST00000360497.4:c.1845-31T= ENSP00000353687.4:n.1845-31T=
ENST00000532133.5:c.1776-31T= ENSP00000435574.1:n.1776-31T=
NM_004621.5:c.2010-31T= NP_004612.2:n.2010-31T=
XM_006718898.2:c.2010-31T= XP_006718961.1:n.2010-31T=
XM_011542968.1:c.1845-31T= XP_011541270.1:n.1845-31T=
XM_011542969.1:c.2010-31T= XP_011541271.1:n.2010-31T=
XM_011542968.3:c.1845-31T= XP_011541270.1:n.1845-31T=
XM_017018221.2:c.1662-31T= XP_016873710.1:n.1662-31T=
XR_001747948.2:n.2366-31T=
NM_004621.6:c.2010-31T= MANE Select NP_004612.2:n.2010-31T=