Canonical Allele Identifier: CA7238822
Community Standard Title: NM_152443.3(RDH12):c.806C>G (p.Ala269Gly)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67729338C>G , CM000676.2:g.67729338C>G GRCh38
NC_000014.8:g.68196055C>G , CM000676.1:g.68196055C>G GRCh37
NC_000014.7:g.67265808C>G NCBI36
NG_008321.1:g.32453C>G

Transcript Alleles

HGVS Amino-acid Change
NM_152443.3:c.806C>G (RDH12) MANE Select NP_689656.2:p.Ala269Gly
ENST00000551171.6:c.806C>G (RDH12) MANE Select ENSP00000449079.1:p.Ala269Gly
NM_152443.2:c.806C>G (RDH12) NP_689656.2:p.Ala269Gly
ENST00000267502.3:c.806C>G (RDH12) ENSP00000267502.3:p.Ala269Gly
ENST00000394455.6:n.3161G>C (ZFYVE26)
ENST00000551171.5:c.806C>G (RDH12) ENSP00000449079.1:p.Ala269Gly
ENST00000552873.1:n.175C>G (RDH12)
XM_017020925.2:c.1313-5857C>G (GPHN) XP_016876414.1:n.1313-5857C>G
XM_017021125.1:c.*404G>C (ZFYVE26) XP_016876614.1:n.*404G>C