Canonical Allele Identifier: CA920063765
Gene: RLN3 HGNC NCBI

Linked Data

dbSNP Id: rs1599542475
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.14029055_14029056del , CM000681.2:g.14029055_14029056del GRCh38
NC_000019.9:g.14139867_14139868del , CM000681.1:g.14139867_14139868del GRCh37
NC_000019.8:g.14000867_14000868del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000431365.3:c.190+661_190+662del MANE Select ENSP00000397415.2:n.190+661_190+662del
ENST00000431365.2:c.190+661_190+662del ENSP00000397415.2:n.190+661_190+662del
ENST00000585987.1:c.190+661_190+662del ENSP00000467130.1:n.190+661_190+662del
NM_001311197.1:c.190+661_190+662del NP_001298126.1:n.190+661_190+662del
NM_080864.2:c.190+661_190+662del NP_543140.1:n.190+661_190+662del
NM_080864.3:c.190+661_190+662del NP_543140.1:n.190+661_190+662del
NM_080864.4:c.190+661_190+662del MANE Select NP_543140.1:n.190+661_190+662del
NM_001311197.2:c.190+661_190+662del NP_001298126.1:n.190+661_190+662del
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