Canonical Allele Identifier: CA403085477

Gene: RETN

Linked Data

• MyVariant Identifiers: chr19:g.7735201G>C (hg19) ; chr19:g.7670315G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7670315G>C , CM000681.2:g.7670315G>C	GRCh38
NC_000019.9:g.7735201G>C , CM000681.1:g.7735201G>C	GRCh37
NC_000019.8:g.7641201G>C	NCBI36
NG_023447.1:g.6230G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000221515.6:c.293G>C MANE Select	ENSP00000221515.1:p.Trp98Ser
ENST00000221515.5:c.293G>C	ENSP00000221515.1:p.Trp98Ser
ENST00000381324.2:c.215G>C	ENSP00000370725.2:p.Trp72Ser
ENST00000629642.1:c.215G>C	ENSP00000485998.1:p.Trp72Ser
NM_001193374.1:c.293G>C	NP_001180303.1:p.Trp98Ser
NM_020415.3:c.293G>C	NP_065148.1:p.Trp98Ser
NM_020415.4:c.293G>C MANE Select	NP_065148.1:p.Trp98Ser
NM_001193374.2:c.293G>C	NP_001180303.1:p.Trp98Ser
NM_001385725.1:c.293G>C	NP_001372654.1:p.Trp98Ser
NM_001385726.1:c.335G>C	NP_001372655.1:p.Trp112Ser
NM_001385727.1:c.215G>C	NP_001372656.1:p.Trp72Ser