Canonical Allele Identifier: CA2793388389

Gene: TRPC6

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101488816dup , CM000673.2:g.101488816dup	GRCh38
NC_000011.9:g.101359547dup , CM000673.1:g.101359547dup	GRCh37
NC_000011.8:g.100864757dup	NCBI36
NG_011476.1:g.100117dup
NG_011476.2:g.100117dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344327.8:c.1293+125dup MANE Select	ENSP00000340913.3:n.1293+125dup
ENST00000344327.7:c.1293+125dup	ENSP00000340913.3:n.1293+125dup
ENST00000348423.8:c.946-5647dup	ENSP00000343672.4:n.946-5647dup
ENST00000360497.4:c.1128+2744dup	ENSP00000353687.4:n.1128+2744dup
ENST00000532133.5:c.1293+125dup	ENSP00000435574.1:n.1293+125dup
NM_004621.5:c.1293+125dup	NP_004612.2:n.1293+125dup
XM_006718898.2:c.1293+125dup	XP_006718961.1:n.1293+125dup
XM_011542968.1:c.1128+125dup	XP_011541270.1:n.1128+125dup
XM_011542969.1:c.1293+125dup	XP_011541271.1:n.1293+125dup
XM_011542968.3:c.1128+125dup	XP_011541270.1:n.1128+125dup
XM_017018221.2:c.946-5647dup	XP_016873710.1:n.946-5647dup
XR_001747948.2:n.1649+125dup
NM_004621.6:c.1293+125dup MANE Select	NP_004612.2:n.1293+125dup