Canonical Allele Identifier: CA1995844675

Gene: TRPC6

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101488814_101488817delinsAAAC , CM000673.2:g.101488814_101488817delinsAAAC	GRCh38
NC_000011.9:g.101359545_101359548delinsAAAC , CM000673.1:g.101359545_101359548delinsAAAC	GRCh37
NC_000011.8:g.100864755_100864758delinsAAAC	NCBI36
NG_011476.1:g.100112_100115delinsGTTT
NG_011476.2:g.100112_100115delinsGTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344327.8:c.1293+120_1293+123delinsGTTT MANE Select	ENSP00000340913.3:n.1293+120_1293+123delinsGTTT
ENST00000344327.7:c.1293+120_1293+123delinsGTTT	ENSP00000340913.3:n.1293+120_1293+123delinsGTTT
ENST00000348423.8:c.946-5652_946-5649delinsGTTT	ENSP00000343672.4:n.946-5652_946-5649delinsGTTT
ENST00000360497.4:c.1128+2739_1128+2742delinsGTTT	ENSP00000353687.4:n.1128+2739_1128+2742delinsGTTT
ENST00000532133.5:c.1293+120_1293+123delinsGTTT	ENSP00000435574.1:n.1293+120_1293+123delinsGTTT
NM_004621.5:c.1293+120_1293+123delinsGTTT	NP_004612.2:n.1293+120_1293+123delinsGTTT
XM_006718898.2:c.1293+120_1293+123delinsGTTT	XP_006718961.1:n.1293+120_1293+123delinsGTTT
XM_011542968.1:c.1128+120_1128+123delinsGTTT	XP_011541270.1:n.1128+120_1128+123delinsGTTT
XM_011542969.1:c.1293+120_1293+123delinsGTTT	XP_011541271.1:n.1293+120_1293+123delinsGTTT
XM_011542968.3:c.1128+120_1128+123delinsGTTT	XP_011541270.1:n.1128+120_1128+123delinsGTTT
XM_017018221.2:c.946-5652_946-5649delinsGTTT	XP_016873710.1:n.946-5652_946-5649delinsGTTT
XR_001747948.2:n.1649+120_1649+123delinsGTTT
NM_004621.6:c.1293+120_1293+123delinsGTTT MANE Select	NP_004612.2:n.1293+120_1293+123delinsGTTT