Canonical Allele Identifier: CA1995839550
Gene: TRPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101483027C= , CM000673.2:g.101483027C= GRCh38
NC_000011.9:g.101353758C= , CM000673.1:g.101353758C= GRCh37
NC_000011.8:g.100858968C= NCBI36
NG_011476.1:g.105902G=
NG_011476.2:g.105902G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344327.8:c.1432G= MANE Select ENSP00000340913.3:p.Asp478=
ENST00000344327.7:c.1432G= ENSP00000340913.3:p.Asp478=
ENST00000348423.8:c.1084G= ENSP00000343672.4:p.Asp362=
ENST00000360497.4:c.1267G= ENSP00000353687.4:p.Asp423=
ENST00000532133.5:c.1432G= ENSP00000435574.1:p.Asp478=
NM_004621.5:c.1432G= NP_004612.2:p.Asp478=
XM_006718898.2:c.1432G= XP_006718961.1:p.Asp478=
XM_011542968.1:c.1267G= XP_011541270.1:p.Asp423=
XM_011542969.1:c.1432G= XP_011541271.1:p.Asp478=
XM_011542968.3:c.1267G= XP_011541270.1:p.Asp423=
XM_017018221.2:c.1084G= XP_016873710.1:p.Asp362=
XR_001747948.2:n.1788G=
NM_004621.6:c.1432G= MANE Select NP_004612.2:p.Asp478=