Canonical Allele Identifier: CA476501131

Gene: TRPC6

Linked Data

• MyVariant Identifiers: chr11:g.101353681T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101482950T>A , CM000673.2:g.101482950T>A	GRCh38
NC_000011.9:g.101353681T>A , CM000673.1:g.101353681T>A	GRCh37
NC_000011.8:g.100858891T>A	NCBI36
NG_011476.1:g.105979A>T
NG_011476.2:g.105979A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000344327.8:c.1509A>T MANE Select	ENSP00000340913.3:p.Ile503=
ENST00000344327.7:c.1509A>T	ENSP00000340913.3:p.Ile503=
ENST00000348423.8:c.1161A>T	ENSP00000343672.4:p.Ile387=
ENST00000360497.4:c.1344A>T	ENSP00000353687.4:p.Ile448=
ENST00000532133.5:c.1509A>T	ENSP00000435574.1:p.Ile503=
NM_004621.5:c.1509A>T	NP_004612.2:p.Ile503=
XM_006718898.2:c.1509A>T	XP_006718961.1:p.Ile503=
XM_011542968.1:c.1344A>T	XP_011541270.1:p.Ile448=
XM_011542969.1:c.1509A>T	XP_011541271.1:p.Ile503=
XM_011542968.3:c.1344A>T	XP_011541270.1:p.Ile448=
XM_017018221.2:c.1161A>T	XP_016873710.1:p.Ile387=
XR_001747948.2:n.1865A>T
NM_004621.6:c.1509A>T MANE Select	NP_004612.2:p.Ile503=