Canonical Allele Identifier: CA10581550
Gene: TRPC6 HGNC NCBI

Linked Data

ClinVar Variation Id: 236178
ClinVar RCV Id: RCV000225046
dbSNP Id: rs878853205
MyVariant Identifiers: chr11:g.101374581G>A (hg19) chr11:g.101503850G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101503850G>A , CM000673.2:g.101503850G>A GRCh38
NC_000011.9:g.101374581G>A , CM000673.1:g.101374581G>A GRCh37
NC_000011.8:g.100879791G>A NCBI36
NG_011476.1:g.85079C>T
NG_011476.2:g.85079C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000344327.8:c.945+174C>T MANE Select ENSP00000340913.3:n.945+174C>T
ENST00000344327.7:c.945+174C>T ENSP00000340913.3:n.945+174C>T
ENST00000348423.8:c.945+174C>T ENSP00000343672.4:n.945+174C>T
ENST00000360497.4:c.945+174C>T ENSP00000353687.4:n.945+174C>T
ENST00000527240.1:n.67+174C>T
ENST00000532133.5:c.945+174C>T ENSP00000435574.1:n.945+174C>T
NM_004621.5:c.945+174C>T NP_004612.2:n.945+174C>T
XM_006718898.2:c.945+174C>T XP_006718961.1:n.945+174C>T
XM_011542968.1:c.780+174C>T XP_011541270.1:n.780+174C>T
XM_011542969.1:c.945+174C>T XP_011541271.1:n.945+174C>T
XM_011542968.3:c.780+174C>T XP_011541270.1:n.780+174C>T
XM_017018221.2:c.945+174C>T XP_016873710.1:n.945+174C>T
XR_001747948.2:n.1301+174C>T
NM_004621.6:c.945+174C>T MANE Select NP_004612.2:n.945+174C>T
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