Canonical Allele Identifier: CA1995891840
Community Standard Title: NM_004621.6(TRPC6):c.171-32777A>T
Gene: TRPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101537575T>A , CM000673.2:g.101537575T>A GRCh38
NC_000011.9:g.101408306T>A , CM000673.1:g.101408306T>A GRCh37
NC_000011.8:g.100913516T>A NCBI36
NG_011476.1:g.51354A>T
NG_011476.2:g.51354A>T

Transcript Alleles

HGVS Amino-acid Change
NM_004621.6:c.171-32777A>T MANE Select NP_004612.2:n.171-32777A>T
ENST00000344327.8:c.171-32777A>T MANE Select ENSP00000340913.3:n.171-32777A>T
NM_004621.5:c.171-32777A>T NP_004612.2:n.171-32777A>T
ENST00000344327.7:c.171-32777A>T ENSP00000340913.3:n.171-32777A>T
ENST00000348423.8:c.171-32777A>T ENSP00000343672.4:n.171-32777A>T
ENST00000360497.4:c.171-32777A>T ENSP00000353687.4:n.171-32777A>T
ENST00000526713.1:n.266-32777A>T
ENST00000532133.5:c.171-32777A>T ENSP00000435574.1:n.171-32777A>T
XM_006718898.2:c.171-32777A>T XP_006718961.1:n.171-32777A>T
XM_011542969.1:c.171-32777A>T XP_011541271.1:n.171-32777A>T
XM_017018221.2:c.171-32777A>T XP_016873710.1:n.171-32777A>T
XR_001747948.2:n.527-32777A>T