Canonical Allele Identifier: CA6244032
Gene: TRPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101453040T>C , CM000673.2:g.101453040T>C GRCh38
NC_000011.9:g.101323771T>C , CM000673.1:g.101323771T>C GRCh37
NC_000011.8:g.100828981T>C NCBI36
NG_011476.1:g.135889A>G
NG_011476.2:g.135889A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344327.8:c.2711A>G MANE Select ENSP00000340913.3:p.Gln904Arg
ENST00000344327.7:c.2711A>G ENSP00000340913.3:p.Gln904Arg
ENST00000348423.8:c.2363A>G ENSP00000343672.4:p.Gln788Arg
ENST00000360497.4:c.2546A>G ENSP00000353687.4:p.Gln849Arg
ENST00000532133.5:c.2477A>G ENSP00000435574.1:p.Gln826Arg
NM_004621.5:c.2711A>G NP_004612.2:p.Gln904Arg
XM_006718898.2:c.2636A>G XP_006718961.1:p.Gln879Arg
XM_011542968.1:c.2546A>G XP_011541270.1:p.Gln849Arg
XM_011542968.3:c.2546A>G XP_011541270.1:p.Gln849Arg
XM_017018221.2:c.2363A>G XP_016873710.1:p.Gln788Arg
XR_001747948.2:n.3068A>G
NM_004621.6:c.2711A>G MANE Select NP_004612.2:p.Gln904Arg