Canonical Allele Identifier: CA110082147
Gene: NPY1R HGNC NCBI

Linked Data

dbSNP Id: rs59293649
gnomAD v2: 4-164245892-GAAA-G
gnomAD v3: 4-163324740-GAAA-G
gnomAD v4: 4-163324740-GAAA-G
MyVariant Identifiers: chr4:g.164245895_164245897del (hg19) chr4:g.164245893_164245895del (hg19) chr4:g.163324743_163324745del (hg38) chr4:g.163324741_163324743del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324752_163324754del , CM000666.2:g.163324752_163324754del GRCh38
NC_000004.11:g.164245904_164245906del , CM000666.1:g.164245904_164245906del GRCh37
NC_000004.10:g.164465354_164465356del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296533.3:c.*560_*562del MANE Select ENSP00000354652.2:n.*560_*562del
ENST00000296533.2:c.*560_*562del ENSP00000354652.2:n.*560_*562del
NM_000909.5:c.*560_*562del NP_000900.1:n.*560_*562del
XM_005263031.2:c.*560_*562del XP_005263088.1:n.*560_*562del
XM_011532010.1:c.*560_*562del XP_011530312.1:n.*560_*562del
XM_005263031.4:c.*560_*562del XP_005263088.1:n.*560_*562del
XM_011532010.3:c.*560_*562del XP_011530312.1:n.*560_*562del
NM_000909.6:c.*560_*562del MANE Select NP_000900.1:n.*560_*562del
Search 100 bp 5'
Search 100 bp 3'