Canonical Allele Identifier: CA1995844761

Gene: TRPC6

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101488899T= , CM000673.2:g.101488899T=	GRCh38
NC_000011.9:g.101359630T= , CM000673.1:g.101359630T=	GRCh37
NC_000011.8:g.100864840T=	NCBI36
NG_011476.1:g.100030A=
NG_011476.2:g.100030A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344327.8:c.1293+38A= MANE Select	ENSP00000340913.3:n.1293+38A=
ENST00000344327.7:c.1293+38A=	ENSP00000340913.3:n.1293+38A=
ENST00000348423.8:c.946-5734A=	ENSP00000343672.4:n.946-5734A=
ENST00000360497.4:c.1128+2657A=	ENSP00000353687.4:n.1128+2657A=
ENST00000532133.5:c.1293+38A=	ENSP00000435574.1:n.1293+38A=
NM_004621.5:c.1293+38A=	NP_004612.2:n.1293+38A=
XM_006718898.2:c.1293+38A=	XP_006718961.1:n.1293+38A=
XM_011542968.1:c.1128+38A=	XP_011541270.1:n.1128+38A=
XM_011542969.1:c.1293+38A=	XP_011541271.1:n.1293+38A=
XM_011542968.3:c.1128+38A=	XP_011541270.1:n.1128+38A=
XM_017018221.2:c.946-5734A=	XP_016873710.1:n.946-5734A=
XR_001747948.2:n.1649+38A=
NM_004621.6:c.1293+38A= MANE Select	NP_004612.2:n.1293+38A=