Canonical Allele Identifier: CA2615685744

Gene: TRPC6

Linked Data

• gnomAD v4: 11-101483029-GTGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101483032_101483034del , CM000673.2:g.101483032_101483034del	GRCh38
NC_000011.9:g.101353763_101353765del , CM000673.1:g.101353763_101353765del	GRCh37
NC_000011.8:g.100858973_100858975del	NCBI36
NG_011476.1:g.105897_105899del
NG_011476.2:g.105897_105899del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344327.8:c.1427_1429del MANE Select	ENSP00000340913.3:p.Ser476del
ENST00000344327.7:c.1427_1429del	ENSP00000340913.3:p.Ser476del
ENST00000348423.8:c.1079_1081del	ENSP00000343672.4:p.Ser360del
ENST00000360497.4:c.1262_1264del	ENSP00000353687.4:p.Ser421del
ENST00000532133.5:c.1427_1429del	ENSP00000435574.1:p.Ser476del
NM_004621.5:c.1427_1429del	NP_004612.2:p.Ser476del
XM_006718898.2:c.1427_1429del	XP_006718961.1:p.Ser476del
XM_011542968.1:c.1262_1264del	XP_011541270.1:p.Ser421del
XM_011542969.1:c.1427_1429del	XP_011541271.1:p.Ser476del
XM_011542968.3:c.1262_1264del	XP_011541270.1:p.Ser421del
XM_017018221.2:c.1079_1081del	XP_016873710.1:p.Ser360del
XR_001747948.2:n.1783_1785del
NM_004621.6:c.1427_1429del MANE Select	NP_004612.2:p.Ser476del