Canonical Allele Identifier: CA1509094320
Gene: NPY1R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324678C= , CM000666.2:g.163324678C= GRCh38
NC_000004.11:g.164245830C= , CM000666.1:g.164245830C= GRCh37
NC_000004.10:g.164465280C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296533.3:c.*625G= MANE Select ENSP00000354652.2:n.*625G=
ENST00000296533.2:c.*625G= ENSP00000354652.2:n.*625G=
NM_000909.5:c.*625G= NP_000900.1:n.*625G=
XM_005263031.2:c.*625G= XP_005263088.1:n.*625G=
XM_011532010.1:c.*625G= XP_011530312.1:n.*625G=
XM_005263031.4:c.*625G= XP_005263088.1:n.*625G=
XM_011532010.3:c.*625G= XP_011530312.1:n.*625G=
NM_000909.6:c.*625G= MANE Select NP_000900.1:n.*625G=
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