Canonical Allele Identifier: CA2615684084
Gene: TRPC6 HGNC NCBI

Linked Data

gnomAD v4: 11-101452784-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101452784G>T , CM000673.2:g.101452784G>T GRCh38
NC_000011.9:g.101323515G>T , CM000673.1:g.101323515G>T GRCh37
NC_000011.8:g.100828725G>T NCBI36
NG_011476.1:g.136145C>A
NG_011476.2:g.136145C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344327.8:c.*171C>A MANE Select ENSP00000340913.3:n.*171C>A
ENST00000344327.7:c.*171C>A ENSP00000340913.3:n.*171C>A
NM_004621.5:c.*171C>A NP_004612.2:n.*171C>A
XM_006718898.2:c.*171C>A XP_006718961.1:n.*171C>A
XM_011542968.1:c.*171C>A XP_011541270.1:n.*171C>A
XM_011542968.3:c.*171C>A XP_011541270.1:n.*171C>A
XM_017018221.2:c.*171C>A XP_016873710.1:n.*171C>A
XR_001747948.2:n.3324C>A
NM_004621.6:c.*171C>A MANE Select NP_004612.2:n.*171C>A
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