Canonical Allele Identifier: CA1995834002
Gene: TRPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101476512T= , CM000673.2:g.101476512T= GRCh38
NC_000011.9:g.101347243T= , CM000673.1:g.101347243T= GRCh37
NC_000011.8:g.100852453T= NCBI36
NG_011476.1:g.112417A=
NG_011476.2:g.112417A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344327.8:c.1533A= MANE Select ENSP00000340913.3:p.Lys511=
ENST00000344327.7:c.1533A= ENSP00000340913.3:p.Lys511=
ENST00000348423.8:c.1185A= ENSP00000343672.4:p.Lys395=
ENST00000360497.4:c.1368A= ENSP00000353687.4:p.Lys456=
ENST00000532133.5:c.1511-2739A= ENSP00000435574.1:n.1511-2739A=
NM_004621.5:c.1533A= NP_004612.2:p.Lys511=
XM_006718898.2:c.1533A= XP_006718961.1:p.Lys511=
XM_011542968.1:c.1368A= XP_011541270.1:p.Lys456=
XM_011542969.1:c.1533A= XP_011541271.1:p.Lys511=
XM_011542968.3:c.1368A= XP_011541270.1:p.Lys456=
XM_017018221.2:c.1185A= XP_016873710.1:p.Lys395=
XR_001747948.2:n.1889A=
NM_004621.6:c.1533A= MANE Select NP_004612.2:p.Lys511=