Canonical Allele Identifier: CA1995885895
Gene: TRPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101453674T= , CM000673.2:g.101453674T= GRCh38
NC_000011.9:g.101324405T= , CM000673.1:g.101324405T= GRCh37
NC_000011.8:g.100829615T= NCBI36
NG_011476.1:g.135255A=
NG_011476.2:g.135255A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344327.8:c.2620A= MANE Select ENSP00000340913.3:p.Lys874=
ENST00000344327.7:c.2620A= ENSP00000340913.3:p.Lys874=
ENST00000348423.8:c.2272A= ENSP00000343672.4:p.Lys758=
ENST00000360497.4:c.2455A= ENSP00000353687.4:p.Lys819=
ENST00000532133.5:c.2386A= ENSP00000435574.1:p.Lys796=
ENST00000532184.1:n.612A=
NM_004621.5:c.2620A= NP_004612.2:p.Lys874=
XM_006718898.2:c.2545A= XP_006718961.1:p.Lys849=
XM_011542968.1:c.2455A= XP_011541270.1:p.Lys819=
XM_011542968.3:c.2455A= XP_011541270.1:p.Lys819=
XM_017018221.2:c.2272A= XP_016873710.1:p.Lys758=
XR_001747948.2:n.2977A=
NM_004621.6:c.2620A= MANE Select NP_004612.2:p.Lys874=