Canonical Allele Identifier: CA2144004326

Gene: RDH12 ZFYVE26 GPHN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67729204C= , CM000676.2:g.67729204C=	GRCh38
NC_000014.8:g.68195921C= , CM000676.1:g.68195921C=	GRCh37
NC_000014.7:g.67265674C=	NCBI36
NG_008321.1:g.32319C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551171.6:c.672C= (RDH12) MANE Select	ENSP00000449079.1:p.Thr224=
ENST00000267502.3:c.672C= (RDH12)	ENSP00000267502.3:p.Thr224=
ENST00000394455.6:n.3288+7G= (ZFYVE26)
ENST00000551171.5:c.672C= (RDH12)	ENSP00000449079.1:p.Thr224=
ENST00000552873.1:n.41C= (RDH12)
NM_152443.2:c.672C= (RDH12)	NP_689656.2:p.Thr224=
XM_017020925.2:c.1313-5991C= (GPHN)	XP_016876414.1:n.1313-5991C=
XM_017021125.1:c.*538G= (ZFYVE26)	XP_016876614.1:n.*538G=
NM_152443.3:c.672C= (RDH12) MANE Select	NP_689656.2:p.Thr224=