Canonical Allele Identifier: CA1995873396

Gene: TRPC6

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101503798A= , CM000673.2:g.101503798A=	GRCh38
NC_000011.9:g.101374529A= , CM000673.1:g.101374529A=	GRCh37
NC_000011.8:g.100879739A=	NCBI36
NG_011476.1:g.85131T=
NG_011476.2:g.85131T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344327.8:c.945+226T= MANE Select	ENSP00000340913.3:n.945+226T=
ENST00000344327.7:c.945+226T=	ENSP00000340913.3:n.945+226T=
ENST00000348423.8:c.945+226T=	ENSP00000343672.4:n.945+226T=
ENST00000360497.4:c.945+226T=	ENSP00000353687.4:n.945+226T=
ENST00000527240.1:n.67+226T=
ENST00000532133.5:c.945+226T=	ENSP00000435574.1:n.945+226T=
NM_004621.5:c.945+226T=	NP_004612.2:n.945+226T=
XM_006718898.2:c.945+226T=	XP_006718961.1:n.945+226T=
XM_011542968.1:c.780+226T=	XP_011541270.1:n.780+226T=
XM_011542969.1:c.945+226T=	XP_011541271.1:n.945+226T=
XM_011542968.3:c.780+226T=	XP_011541270.1:n.780+226T=
XM_017018221.2:c.945+226T=	XP_016873710.1:n.945+226T=
XR_001747948.2:n.1301+226T=
NM_004621.6:c.945+226T= MANE Select	NP_004612.2:n.945+226T=