Canonical Allele Identifier: CA1995874975
Gene: TRPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101504541T= , CM000673.2:g.101504541T= GRCh38
NC_000011.9:g.101375272T= , CM000673.1:g.101375272T= GRCh37
NC_000011.8:g.100880482T= NCBI36
NG_011476.1:g.84388A=
NG_011476.2:g.84388A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344327.8:c.428A= MANE Select ENSP00000340913.3:p.Asn143=
ENST00000344327.7:c.428A= ENSP00000340913.3:p.Asn143=
ENST00000348423.8:c.428A= ENSP00000343672.4:p.Asn143=
ENST00000360497.4:c.428A= ENSP00000353687.4:p.Asn143=
ENST00000532133.5:c.428A= ENSP00000435574.1:p.Asn143=
NM_004621.5:c.428A= NP_004612.2:p.Asn143=
XM_006718898.2:c.428A= XP_006718961.1:p.Asn143=
XM_011542968.1:c.263A= XP_011541270.1:p.Asn88=
XM_011542969.1:c.428A= XP_011541271.1:p.Asn143=
XM_011542968.3:c.263A= XP_011541270.1:p.Asn88=
XM_017018221.2:c.428A= XP_016873710.1:p.Asn143=
XR_001747948.2:n.784A=
NM_004621.6:c.428A= MANE Select NP_004612.2:p.Asn143=