Canonical Allele Identifier: CA382440302

Gene: TRPC6

Linked Data

• MyVariant Identifiers: chr11:g.101344393C>G (hg19) ; chr11:g.101473662C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101473662C>G , CM000673.2:g.101473662C>G	GRCh38
NC_000011.9:g.101344393C>G , CM000673.1:g.101344393C>G	GRCh37
NC_000011.8:g.100849603C>G	NCBI36
NG_011476.1:g.115267G>C
NG_011476.2:g.115267G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344327.8:c.1856G>C MANE Select	ENSP00000340913.3:p.Ser619Thr
ENST00000344327.7:c.1856G>C	ENSP00000340913.3:p.Ser619Thr
ENST00000348423.8:c.1508G>C	ENSP00000343672.4:p.Ser503Thr
ENST00000360497.4:c.1691G>C	ENSP00000353687.4:p.Ser564Thr
ENST00000532133.5:c.1622G>C	ENSP00000435574.1:p.Ser541Thr
NM_004621.5:c.1856G>C	NP_004612.2:p.Ser619Thr
XM_006718898.2:c.1856G>C	XP_006718961.1:p.Ser619Thr
XM_011542968.1:c.1691G>C	XP_011541270.1:p.Ser564Thr
XM_011542969.1:c.1856G>C	XP_011541271.1:p.Ser619Thr
XM_011542968.3:c.1691G>C	XP_011541270.1:p.Ser564Thr
XM_017018221.2:c.1508G>C	XP_016873710.1:p.Ser503Thr
XR_001747948.2:n.2212G>C
NM_004621.6:c.1856G>C MANE Select	NP_004612.2:p.Ser619Thr