Canonical Allele Identifier: CA390154226

Gene: RDH12 ZFYVE26 GPHN

Linked Data

• dbSNP Id: rs878853339
• MyVariant Identifiers: chr14:g.68200524T>A (hg19) ; chr14:g.67733807T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67733807T>A , CM000676.2:g.67733807T>A	GRCh38
NC_000014.8:g.68200524T>A , CM000676.1:g.68200524T>A	GRCh37
NC_000014.7:g.67270277T>A	NCBI36
NG_008321.1:g.36922T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551171.6:c.910T>A (RDH12) MANE Select	ENSP00000449079.1:p.Trp304Arg
ENST00000267502.3:c.910T>A (RDH12)	ENSP00000267502.3:p.Trp304Arg
ENST00000394455.6:n.2680-3988A>T (ZFYVE26)
ENST00000551171.5:c.910T>A (RDH12)	ENSP00000449079.1:p.Trp304Arg
NM_152443.2:c.910T>A (RDH12)	NP_689656.2:p.Trp304Arg
XM_006720093.2:c.7417-3988A>T (ZFYVE26)	XP_006720156.1:n.7417-3988A>T
XM_017020925.2:c.1313-1388T>A (GPHN)	XP_016876414.1:n.1313-1388T>A
XM_017021125.1:c.7435-3988A>T (ZFYVE26)	XP_016876614.1:n.7435-3988A>T
NM_152443.3:c.910T>A (RDH12) MANE Select	NP_689656.2:p.Trp304Arg