Canonical Allele Identifier: CA1995844635

Gene: TRPC6

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101488741_101488743delinsCAT , CM000673.2:g.101488741_101488743delinsCAT	GRCh38
NC_000011.9:g.101359472_101359474delinsCAT , CM000673.1:g.101359472_101359474delinsCAT	GRCh37
NC_000011.8:g.100864682_100864684delinsCAT	NCBI36
NG_011476.1:g.100186_100188delinsATG
NG_011476.2:g.100186_100188delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344327.8:c.1293+194_1293+196delinsATG MANE Select	ENSP00000340913.3:n.1293+194_1293+196delinsATG
ENST00000344327.7:c.1293+194_1293+196delinsATG	ENSP00000340913.3:n.1293+194_1293+196delinsATG
ENST00000348423.8:c.946-5578_946-5576delinsATG	ENSP00000343672.4:n.946-5578_946-5576delinsATG
ENST00000360497.4:c.1128+2813_1128+2815delinsATG	ENSP00000353687.4:n.1128+2813_1128+2815delinsATG
ENST00000532133.5:c.1293+194_1293+196delinsATG	ENSP00000435574.1:n.1293+194_1293+196delinsATG
NM_004621.5:c.1293+194_1293+196delinsATG	NP_004612.2:n.1293+194_1293+196delinsATG
XM_006718898.2:c.1293+194_1293+196delinsATG	XP_006718961.1:n.1293+194_1293+196delinsATG
XM_011542968.1:c.1128+194_1128+196delinsATG	XP_011541270.1:n.1128+194_1128+196delinsATG
XM_011542969.1:c.1293+194_1293+196delinsATG	XP_011541271.1:n.1293+194_1293+196delinsATG
XM_011542968.3:c.1128+194_1128+196delinsATG	XP_011541270.1:n.1128+194_1128+196delinsATG
XM_017018221.2:c.946-5578_946-5576delinsATG	XP_016873710.1:n.946-5578_946-5576delinsATG
XR_001747948.2:n.1649+194_1649+196delinsATG
NM_004621.6:c.1293+194_1293+196delinsATG MANE Select	NP_004612.2:n.1293+194_1293+196delinsATG