Canonical Allele Identifier: CA631313539
Gene: RETN HGNC NCBI

Linked Data

dbSNP Id: rs1458081290
gnomAD v2: 19-7733958-C-CG
gnomAD v3: 19-7669072-C-CG
gnomAD v4: 19-7669072-C-CG
MyVariant Identifiers: chr19:g.7733958_7733959insG (hg19) chr19:g.7669072_7669073insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7669074dup , CM000681.2:g.7669074dup GRCh38
NC_000019.9:g.7733960dup , CM000681.1:g.7733960dup GRCh37
NC_000019.8:g.7639960dup NCBI36
NG_023447.1:g.4989dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000221515.6:c.-58dup MANE Select ENSP00000221515.1:n.-58dup
ENST00000221515.5:c.-58dup ENSP00000221515.1:n.-58dup
NM_020415.4:c.-58dup MANE Select NP_065148.1:n.-58dup
NM_001193374.2:c.-49dup NP_001180303.1:n.-49dup
NM_001385725.1:c.-102dup NP_001372654.1:n.-102dup
NM_001385726.1:c.-58dup NP_001372655.1:n.-58dup
NM_001385727.1:c.-58dup NP_001372656.1:n.-58dup
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