Canonical Allele Identifier: CA476501259

Gene: TRPC6

Linked Data

• MyVariant Identifiers: chr11:g.101353762G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101483031G>A , CM000673.2:g.101483031G>A	GRCh38
NC_000011.9:g.101353762G>A , CM000673.1:g.101353762G>A	GRCh37
NC_000011.8:g.100858972G>A	NCBI36
NG_011476.1:g.105898C>T
NG_011476.2:g.105898C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000344327.8:c.1428C>T MANE Select	ENSP00000340913.3:p.Ser476=
ENST00000344327.7:c.1428C>T	ENSP00000340913.3:p.Ser476=
ENST00000348423.8:c.1080C>T	ENSP00000343672.4:p.Ser360=
ENST00000360497.4:c.1263C>T	ENSP00000353687.4:p.Ser421=
ENST00000532133.5:c.1428C>T	ENSP00000435574.1:p.Ser476=
NM_004621.5:c.1428C>T	NP_004612.2:p.Ser476=
XM_006718898.2:c.1428C>T	XP_006718961.1:p.Ser476=
XM_011542968.1:c.1263C>T	XP_011541270.1:p.Ser421=
XM_011542969.1:c.1428C>T	XP_011541271.1:p.Ser476=
XM_011542968.3:c.1263C>T	XP_011541270.1:p.Ser421=
XM_017018221.2:c.1080C>T	XP_016873710.1:p.Ser360=
XR_001747948.2:n.1784C>T
NM_004621.6:c.1428C>T MANE Select	NP_004612.2:p.Ser476=