Canonical Allele Identifier: CA10629679

Gene: TRPC6

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101452246_101452247insAATA , CM000673.2:g.101452246_101452247insAATA	GRCh38
NC_000011.9:g.101322977_101322978insAATA , CM000673.1:g.101322977_101322978insAATA	GRCh37
NC_000011.8:g.100828187_100828188insAATA	NCBI36
NG_011476.1:g.136684_136685insTTTA
NG_011476.2:g.136684_136685insTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344327.8:c.*710_*711insTTTA MANE Select	ENSP00000340913.3:n.*710_*711insTTTA
ENST00000344327.7:c.*710_*711insTTTA	ENSP00000340913.3:n.*710_*711insTTTA
NM_004621.5:c.*710_*711insTTTA	NP_004612.2:n.*710_*711insTTTA
XM_006718898.2:c.*710_*711insTTTA	XP_006718961.1:n.*710_*711insTTTA
XM_011542968.1:c.*710_*711insTTTA	XP_011541270.1:n.*710_*711insTTTA
XR_947953.1:n.3138_3139insAATA
XM_011542968.3:c.*710_*711insTTTA	XP_011541270.1:n.*710_*711insTTTA
XM_017018221.2:c.*710_*711insTTTA	XP_016873710.1:n.*710_*711insTTTA
XR_001747948.2:n.3863_3864insTTTA
NM_004621.6:c.*710_*711insTTTA MANE Select	NP_004612.2:n.*710_*711insTTTA