Canonical Allele Identifier: CA1995844957
Community Standard Title: NM_004621.6(TRPC6):c.1211C= (p.Ala404=)
Gene: TRPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101489019G= , CM000673.2:g.101489019G= GRCh38
NC_000011.9:g.101359750G= , CM000673.1:g.101359750G= GRCh37
NC_000011.8:g.100864960G= NCBI36
NG_011476.1:g.99910C=
NG_011476.2:g.99910C=

Transcript Alleles

HGVS Amino-acid Change
NM_004621.6:c.1211C= MANE Select NP_004612.2:p.Ala404=
ENST00000344327.8:c.1211C= MANE Select ENSP00000340913.3:p.Ala404=
NM_004621.5:c.1211C= NP_004612.2:p.Ala404=
ENST00000344327.7:c.1211C= ENSP00000340913.3:p.Ala404=
ENST00000348423.8:c.946-5854C= ENSP00000343672.4:n.946-5854C=
ENST00000360497.4:c.1128+2537C= ENSP00000353687.4:n.1128+2537C=
ENST00000532133.5:c.1211C= ENSP00000435574.1:p.Ala404=
XM_006718898.2:c.1211C= XP_006718961.1:p.Ala404=
XM_011542968.1:c.1046C= XP_011541270.1:p.Ala349=
XM_011542968.3:c.1046C= XP_011541270.1:p.Ala349=
XM_011542969.1:c.1211C= XP_011541271.1:p.Ala404=
XM_017018221.2:c.946-5854C= XP_016873710.1:n.946-5854C=
XR_001747948.2:n.1567C=