Canonical Allele Identifier: CA15720878
Gene: TRPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101453252G>A , CM000673.2:g.101453252G>A GRCh38
NC_000011.9:g.101323983G>A , CM000673.1:g.101323983G>A GRCh37
NC_000011.8:g.100829193G>A NCBI36
NG_011476.1:g.135677C>T
NG_011476.2:g.135677C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344327.8:c.2645-146C>T MANE Select ENSP00000340913.3:n.2645-146C>T
ENST00000344327.7:c.2645-146C>T ENSP00000340913.3:n.2645-146C>T
ENST00000348423.8:c.2297-146C>T ENSP00000343672.4:n.2297-146C>T
ENST00000360497.4:c.2480-146C>T ENSP00000353687.4:n.2480-146C>T
ENST00000532133.5:c.2411-146C>T ENSP00000435574.1:n.2411-146C>T
NM_004621.5:c.2645-146C>T NP_004612.2:n.2645-146C>T
XM_006718898.2:c.2570-146C>T XP_006718961.1:n.2570-146C>T
XM_011542968.1:c.2480-146C>T XP_011541270.1:n.2480-146C>T
XM_011542968.3:c.2480-146C>T XP_011541270.1:n.2480-146C>T
XM_017018221.2:c.2297-146C>T XP_016873710.1:n.2297-146C>T
XR_001747948.2:n.3002-146C>T
NM_004621.6:c.2645-146C>T MANE Select NP_004612.2:n.2645-146C>T