Canonical Allele Identifier: CA2321035951

Gene: RETN

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7670313C= , CM000681.2:g.7670313C=	GRCh38
NC_000019.9:g.7735199C= , CM000681.1:g.7735199C=	GRCh37
NC_000019.8:g.7641199C=	NCBI36
NG_023447.1:g.6228C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000221515.6:c.291C= MANE Select	ENSP00000221515.1:p.Asp97=
ENST00000221515.5:c.291C=	ENSP00000221515.1:p.Asp97=
ENST00000381324.2:c.213C=	ENSP00000370725.2:p.Asp71=
ENST00000629642.1:c.213C=	ENSP00000485998.1:p.Asp71=
NM_001193374.1:c.291C=	NP_001180303.1:p.Asp97=
NM_020415.3:c.291C=	NP_065148.1:p.Asp97=
NM_020415.4:c.291C= MANE Select	NP_065148.1:p.Asp97=
NM_001193374.2:c.291C=	NP_001180303.1:p.Asp97=
NM_001385725.1:c.291C=	NP_001372654.1:p.Asp97=
NM_001385726.1:c.333C=	NP_001372655.1:p.Asp111=
NM_001385727.1:c.213C=	NP_001372656.1:p.Asp71=