Canonical Allele Identifier: CA403085488

Gene: RETN

Linked Data

• MyVariant Identifiers: chr19:g.7735203A>T (hg19) ; chr19:g.7670317A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7670317A>T , CM000681.2:g.7670317A>T	GRCh38
NC_000019.9:g.7735203A>T , CM000681.1:g.7735203A>T	GRCh37
NC_000019.8:g.7641203A>T	NCBI36
NG_023447.1:g.6232A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000221515.6:c.295A>T MANE Select	ENSP00000221515.1:p.Thr99Ser
ENST00000221515.5:c.295A>T	ENSP00000221515.1:p.Thr99Ser
ENST00000381324.2:c.217A>T	ENSP00000370725.2:p.Thr73Ser
ENST00000629642.1:c.217A>T	ENSP00000485998.1:p.Thr73Ser
NM_001193374.1:c.295A>T	NP_001180303.1:p.Thr99Ser
NM_020415.3:c.295A>T	NP_065148.1:p.Thr99Ser
NM_020415.4:c.295A>T MANE Select	NP_065148.1:p.Thr99Ser
NM_001193374.2:c.295A>T	NP_001180303.1:p.Thr99Ser
NM_001385725.1:c.295A>T	NP_001372654.1:p.Thr99Ser
NM_001385726.1:c.337A>T	NP_001372655.1:p.Thr113Ser
NM_001385727.1:c.217A>T	NP_001372656.1:p.Thr73Ser