Canonical Allele Identifier: CA1995839408

Gene: TRPC6

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101482921G= , CM000673.2:g.101482921G=	GRCh38
NC_000011.9:g.101353652G= , CM000673.1:g.101353652G=	GRCh37
NC_000011.8:g.100858862G=	NCBI36
NG_011476.1:g.106008C=
NG_011476.2:g.106008C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000344327.8:c.1510+28C= MANE Select	ENSP00000340913.3:n.1510+28C=
ENST00000344327.7:c.1510+28C=	ENSP00000340913.3:n.1510+28C=
ENST00000348423.8:c.1162+28C=	ENSP00000343672.4:n.1162+28C=
ENST00000360497.4:c.1345+28C=	ENSP00000353687.4:n.1345+28C=
ENST00000532133.5:c.1510+28C=	ENSP00000435574.1:n.1510+28C=
NM_004621.5:c.1510+28C=	NP_004612.2:n.1510+28C=
XM_006718898.2:c.1510+28C=	XP_006718961.1:n.1510+28C=
XM_011542968.1:c.1345+28C=	XP_011541270.1:n.1345+28C=
XM_011542969.1:c.1510+28C=	XP_011541271.1:n.1510+28C=
XM_011542968.3:c.1345+28C=	XP_011541270.1:n.1345+28C=
XM_017018221.2:c.1162+28C=	XP_016873710.1:n.1162+28C=
XR_001747948.2:n.1866+28C=
NM_004621.6:c.1510+28C= MANE Select	NP_004612.2:n.1510+28C=