Canonical Allele Identifier: CA2321035535

Gene: RETN

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7669625G= , CM000681.2:g.7669625G=	GRCh38
NC_000019.9:g.7734511G= , CM000681.1:g.7734511G=	GRCh37
NC_000019.8:g.7640511G=	NCBI36
NG_023447.1:g.5540G=

Transcript Alleles

HGVS	Amino-acid Change
NM_020415.4:c.118+181G= MANE Select	NP_065148.1:n.118+181G=
ENST00000221515.6:c.118+181G= MANE Select	ENSP00000221515.1:n.118+181G=
NM_001193374.1:c.118+181G=	NP_001180303.1:n.118+181G=
NM_001193374.2:c.118+181G=	NP_001180303.1:n.118+181G=
NM_001385725.1:c.118+181G=	NP_001372654.1:n.118+181G=
NM_001385726.1:c.118+181G=	NP_001372655.1:n.118+181G=
NM_001385727.1:c.118+181G=	NP_001372656.1:n.118+181G=
NM_020415.3:c.118+181G=	NP_065148.1:n.118+181G=
ENST00000221515.5:c.118+181G=	ENSP00000221515.1:n.118+181G=
ENST00000381324.2:c.118+181G=	ENSP00000370725.2:n.118+181G=
ENST00000629642.1:c.118+181G=	ENSP00000485998.1:n.118+181G=