Canonical Allele Identifier: CA7238794
Community Standard Title: NM_152443.3(RDH12):c.697G>C (p.Val233Leu)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67729229G>C , CM000676.2:g.67729229G>C GRCh38
NC_000014.8:g.68195946G>C , CM000676.1:g.68195946G>C GRCh37
NC_000014.7:g.67265699G>C NCBI36
NG_008321.1:g.32344G>C

Transcript Alleles

HGVS Amino-acid Change
NM_152443.3:c.697G>C (RDH12) MANE Select NP_689656.2:p.Val233Leu
ENST00000551171.6:c.697G>C (RDH12) MANE Select ENSP00000449079.1:p.Val233Leu
NM_152443.2:c.697G>C (RDH12) NP_689656.2:p.Val233Leu
ENST00000267502.3:c.697G>C (RDH12) ENSP00000267502.3:p.Val233Leu
ENST00000394455.6:n.3270C>G (ZFYVE26)
ENST00000551171.5:c.697G>C (RDH12) ENSP00000449079.1:p.Val233Leu
ENST00000552873.1:n.66G>C (RDH12)
XM_017020925.2:c.1313-5966G>C (GPHN) XP_016876414.1:n.1313-5966G>C
XM_017021125.1:c.*513C>G (ZFYVE26) XP_016876614.1:n.*513C>G