Canonical Allele Identifier: CA2768877954
Gene: PDE6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149896896T>C , CM000667.2:g.149896896T>C GRCh38
NC_000005.9:g.149276459T>C , CM000667.1:g.149276459T>C GRCh37
NC_000005.8:g.149256652T>C NCBI36
NG_009102.1:g.52898A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000255266.10:c.1408-120A>G MANE Select ENSP00000255266.5:n.1408-120A>G
ENST00000255266.9:c.1408-120A>G ENSP00000255266.5:n.1408-120A>G
ENST00000508173.5:n.1384-120A>G
ENST00000613228.1:c.1165-120A>G ENSP00000478060.1:n.1165-120A>G
ENST00000617647.4:c.1165-120A>G ENSP00000482774.1:n.1165-120A>G
NM_000440.2:c.1408-120A>G NP_000431.2:n.1408-120A>G
XM_011537648.1:c.1408-120A>G XP_011535950.1:n.1408-120A>G
XM_011537649.1:c.862-120A>G XP_011535951.1:n.862-120A>G
XM_011537650.1:c.523-120A>G XP_011535952.1:n.523-120A>G
XM_011537651.1:c.361-120A>G XP_011535953.1:n.361-120A>G
XM_011537652.1:c.331-120A>G XP_011535954.1:n.331-120A>G
XM_011537653.1:c.331-120A>G XP_011535955.1:n.331-120A>G
XM_011537654.1:c.331-120A>G XP_011535956.1:n.331-120A>G
XM_011537650.2:c.523-120A>G XP_011535952.1:n.523-120A>G
XM_011537651.2:c.361-120A>G XP_011535953.1:n.361-120A>G
XM_011537653.2:c.331-120A>G XP_011535955.1:n.331-120A>G
XM_011537654.2:c.331-120A>G XP_011535956.1:n.331-120A>G
XM_017009572.2:c.1165-120A>G XP_016865061.1:n.1165-120A>G
NM_000440.3:c.1408-120A>G MANE Select NP_000431.2:n.1408-120A>G