Canonical Allele Identifier: CA1995898988

Gene: TRPC6

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101472200C= , CM000673.2:g.101472200C=	GRCh38
NC_000011.9:g.101342931C= , CM000673.1:g.101342931C=	GRCh37
NC_000011.8:g.100848141C=	NCBI36
NG_011476.1:g.116729G=
NG_011476.2:g.116729G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344327.8:c.2142G= MANE Select	ENSP00000340913.3:p.Thr714=
ENST00000344327.7:c.2142G=	ENSP00000340913.3:p.Thr714=
ENST00000348423.8:c.1794G=	ENSP00000343672.4:p.Thr598=
ENST00000360497.4:c.1977G=	ENSP00000353687.4:p.Thr659=
ENST00000532133.5:c.1908G=	ENSP00000435574.1:p.Thr636=
NM_004621.5:c.2142G=	NP_004612.2:p.Thr714=
XM_006718898.2:c.2142G=	XP_006718961.1:p.Thr714=
XM_011542968.1:c.1977G=	XP_011541270.1:p.Thr659=
XM_011542969.1:c.2142G=	XP_011541271.1:p.Thr714=
XM_011542968.3:c.1977G=	XP_011541270.1:p.Thr659=
XM_017018221.2:c.1794G=	XP_016873710.1:p.Thr598=
XR_001747948.2:n.2498G=
NM_004621.6:c.2142G= MANE Select	NP_004612.2:p.Thr714=