Canonical Allele Identifier: CA1069773496
Gene: NPY2R HGNC NCBI

Linked Data

dbSNP Id: rs1729364537
gnomAD v3: 4-155209811-GAT-G
gnomAD v4: 4-155209811-GAT-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.155209812_155209813del , CM000666.2:g.155209812_155209813del GRCh38
NC_000004.11:g.156130964_156130965del , CM000666.1:g.156130964_156130965del GRCh37
NC_000004.10:g.156350414_156350415del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000329476.4:c.-49+743_-49+744del MANE Select ENSP00000332591.3:n.-49+743_-49+744del
ENST00000329476.3:c.-49+743_-49+744del ENSP00000332591.3:n.-49+743_-49+744del
ENST00000506608.1:c.-49+747_-49+748del ENSP00000426366.1:n.-49+747_-49+748del
NM_000910.3:c.-49+743_-49+744del NP_000901.1:n.-49+743_-49+744del
XM_005263033.3:c.-48-4080_-48-4079del XP_005263090.1:n.-48-4080_-48-4079del
XM_005263034.3:c.-49+747_-49+748del XP_005263091.1:n.-49+747_-49+748del
XM_005263033.4:c.-48-4080_-48-4079del XP_005263090.1:n.-48-4080_-48-4079del
XM_005263034.4:c.-49+747_-49+748del XP_005263091.1:n.-49+747_-49+748del
NM_000910.4:c.-49+743_-49+744del MANE Select NP_000901.1:n.-49+743_-49+744del
NM_001370180.1:c.-49+747_-49+748del NP_001357109.1:n.-49+747_-49+748del
NM_001375470.1:c.-48-4080_-48-4079del NP_001362399.1:n.-48-4080_-48-4079del
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