Canonical Allele Identifier: CA2764320504
Gene: NPY1R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324600G>A , CM000666.2:g.163324600G>A GRCh38
NC_000004.11:g.164245752G>A , CM000666.1:g.164245752G>A GRCh37
NC_000004.10:g.164465202G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296533.3:c.*703C>T MANE Select ENSP00000354652.2:n.*703C>T
ENST00000296533.2:c.*703C>T ENSP00000354652.2:n.*703C>T
NM_000909.5:c.*703C>T NP_000900.1:n.*703C>T
XM_005263031.2:c.*703C>T XP_005263088.1:n.*703C>T
XM_011532010.1:c.*703C>T XP_011530312.1:n.*703C>T
XM_005263031.4:c.*703C>T XP_005263088.1:n.*703C>T
XM_011532010.3:c.*703C>T XP_011530312.1:n.*703C>T
NM_000909.6:c.*703C>T MANE Select NP_000900.1:n.*703C>T
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