Canonical Allele Identifier: CA1070340531
Gene: NPY1R HGNC NCBI

Linked Data

dbSNP Id: rs1734561260
gnomAD v3: 4-163324576-T-G
gnomAD v4: 4-163324576-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324576T>G , CM000666.2:g.163324576T>G GRCh38
NC_000004.11:g.164245728T>G , CM000666.1:g.164245728T>G GRCh37
NC_000004.10:g.164465178T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296533.3:c.*727A>C MANE Select ENSP00000354652.2:n.*727A>C
ENST00000296533.2:c.*727A>C ENSP00000354652.2:n.*727A>C
NM_000909.5:c.*727A>C NP_000900.1:n.*727A>C
XM_005263031.2:c.*727A>C XP_005263088.1:n.*727A>C
XM_011532010.1:c.*727A>C XP_011530312.1:n.*727A>C
XM_005263031.4:c.*727A>C XP_005263088.1:n.*727A>C
XM_011532010.3:c.*727A>C XP_011530312.1:n.*727A>C
NM_000909.6:c.*727A>C MANE Select NP_000900.1:n.*727A>C
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