Canonical Allele Identifier: CA403085479
Gene: RETN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7670316G>A , CM000681.2:g.7670316G>A GRCh38
NC_000019.9:g.7735202G>A , CM000681.1:g.7735202G>A GRCh37
NC_000019.8:g.7641202G>A NCBI36
NG_023447.1:g.6231G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000221515.6:c.294G>A MANE Select ENSP00000221515.1:p.Trp98Ter
ENST00000221515.5:c.294G>A ENSP00000221515.1:p.Trp98Ter
ENST00000381324.2:c.216G>A ENSP00000370725.2:p.Trp72Ter
ENST00000629642.1:c.216G>A ENSP00000485998.1:p.Trp72Ter
NM_001193374.1:c.294G>A NP_001180303.1:p.Trp98Ter
NM_020415.3:c.294G>A NP_065148.1:p.Trp98Ter
NM_020415.4:c.294G>A MANE Select NP_065148.1:p.Trp98Ter
NM_001193374.2:c.294G>A NP_001180303.1:p.Trp98Ter
NM_001385725.1:c.294G>A NP_001372654.1:p.Trp98Ter
NM_001385726.1:c.336G>A NP_001372655.1:p.Trp112Ter
NM_001385727.1:c.216G>A NP_001372656.1:p.Trp72Ter