Canonical Allele Identifier: CA2615685834

Gene: TRPC6

Linked Data

• gnomAD v4: 11-101488809-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101488809G>T , CM000673.2:g.101488809G>T	GRCh38
NC_000011.9:g.101359540G>T , CM000673.1:g.101359540G>T	GRCh37
NC_000011.8:g.100864750G>T	NCBI36
NG_011476.1:g.100120C>A
NG_011476.2:g.100120C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344327.8:c.1293+128C>A MANE Select	ENSP00000340913.3:n.1293+128C>A
ENST00000344327.7:c.1293+128C>A	ENSP00000340913.3:n.1293+128C>A
ENST00000348423.8:c.946-5644C>A	ENSP00000343672.4:n.946-5644C>A
ENST00000360497.4:c.1128+2747C>A	ENSP00000353687.4:n.1128+2747C>A
ENST00000532133.5:c.1293+128C>A	ENSP00000435574.1:n.1293+128C>A
NM_004621.5:c.1293+128C>A	NP_004612.2:n.1293+128C>A
XM_006718898.2:c.1293+128C>A	XP_006718961.1:n.1293+128C>A
XM_011542968.1:c.1128+128C>A	XP_011541270.1:n.1128+128C>A
XM_011542969.1:c.1293+128C>A	XP_011541271.1:n.1293+128C>A
XM_011542968.3:c.1128+128C>A	XP_011541270.1:n.1128+128C>A
XM_017018221.2:c.946-5644C>A	XP_016873710.1:n.946-5644C>A
XR_001747948.2:n.1649+128C>A
NM_004621.6:c.1293+128C>A MANE Select	NP_004612.2:n.1293+128C>A