Canonical Allele Identifier: CA2144004297
Gene: RDH12 HGNC NCBI
ZFYVE26 HGNC NCBI
GPHN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67729153A= , CM000676.2:g.67729153A= GRCh38
NC_000014.8:g.68195870A= , CM000676.1:g.68195870A= GRCh37
NC_000014.7:g.67265623A= NCBI36
NG_008321.1:g.32268A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000551171.6:c.659-38A= (RDH12) MANE Select ENSP00000449079.1:n.659-38A=
ENST00000267502.3:c.659-38A= (RDH12) ENSP00000267502.3:n.659-38A=
ENST00000394455.6:n.3288+58T= (ZFYVE26)
ENST00000551171.5:c.659-38A= (RDH12) ENSP00000449079.1:n.659-38A=
ENST00000552873.1:n.28-38A= (RDH12)
NM_152443.2:c.659-38A= (RDH12) NP_689656.2:n.659-38A=
XM_017020925.2:c.1313-6042A= (GPHN) XP_016876414.1:n.1313-6042A=
XM_017021125.1:c.*589T= (ZFYVE26) XP_016876614.1:n.*589T=
NM_152443.3:c.659-38A= (RDH12) MANE Select NP_689656.2:n.659-38A=
Search 100 bp 5'
Search 100 bp 3'