Canonical Allele Identifier: CA7238795
Community Standard Title: NM_152443.3(RDH12):c.698T>A (p.Val233Asp)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67729230T>A , CM000676.2:g.67729230T>A GRCh38
NC_000014.8:g.68195947T>A , CM000676.1:g.68195947T>A GRCh37
NC_000014.7:g.67265700T>A NCBI36
NG_008321.1:g.32345T>A

Transcript Alleles

HGVS Amino-acid Change
NM_152443.3:c.698T>A (RDH12) MANE Select NP_689656.2:p.Val233Asp
ENST00000551171.6:c.698T>A (RDH12) MANE Select ENSP00000449079.1:p.Val233Asp
NM_152443.2:c.698T>A (RDH12) NP_689656.2:p.Val233Asp
ENST00000267502.3:c.698T>A (RDH12) ENSP00000267502.3:p.Val233Asp
ENST00000394455.6:n.3269A>T (ZFYVE26)
ENST00000551171.5:c.698T>A (RDH12) ENSP00000449079.1:p.Val233Asp
ENST00000552873.1:n.67T>A (RDH12)
XM_017020925.2:c.1313-5965T>A (GPHN) XP_016876414.1:n.1313-5965T>A
XM_017021125.1:c.*512A>T (ZFYVE26) XP_016876614.1:n.*512A>T