Canonical Allele Identifier: CA783524200

Gene: RLN3

Linked Data

• dbSNP Id: rs1328938449
• gnomAD v3: 19-14029145-CAG-C
• gnomAD v4: 19-14029145-CAG-C
• MyVariant Identifiers: chr19:g.14139958_14139959del (hg19) ; chr19:g.14029146_14029147del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.14029148_14029149del , CM000681.2:g.14029148_14029149del	GRCh38
NC_000019.9:g.14139960_14139961del , CM000681.1:g.14139960_14139961del	GRCh37
NC_000019.8:g.14000960_14000961del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000431365.3:c.190+754_190+755del MANE Select	ENSP00000397415.2:n.190+754_190+755del
ENST00000431365.2:c.190+754_190+755del	ENSP00000397415.2:n.190+754_190+755del
ENST00000585987.1:c.190+754_190+755del	ENSP00000467130.1:n.190+754_190+755del
NM_001311197.1:c.190+754_190+755del	NP_001298126.1:n.190+754_190+755del
NM_080864.2:c.190+754_190+755del	NP_543140.1:n.190+754_190+755del
NM_080864.3:c.190+754_190+755del	NP_543140.1:n.190+754_190+755del
NM_080864.4:c.190+754_190+755del MANE Select	NP_543140.1:n.190+754_190+755del
NM_001311197.2:c.190+754_190+755del	NP_001298126.1:n.190+754_190+755del