Canonical Allele Identifier: CA2672548306
Gene: NPY1R HGNC NCBI

Linked Data

gnomAD v4: 4-163324562-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324562C>A , CM000666.2:g.163324562C>A GRCh38
NC_000004.11:g.164245714C>A , CM000666.1:g.164245714C>A GRCh37
NC_000004.10:g.164465164C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296533.3:c.*741G>T MANE Select ENSP00000354652.2:n.*741G>T
ENST00000296533.2:c.*741G>T ENSP00000354652.2:n.*741G>T
NM_000909.5:c.*741G>T NP_000900.1:n.*741G>T
XM_005263031.2:c.*741G>T XP_005263088.1:n.*741G>T
XM_011532010.1:c.*741G>T XP_011530312.1:n.*741G>T
XM_005263031.4:c.*741G>T XP_005263088.1:n.*741G>T
XM_011532010.3:c.*741G>T XP_011530312.1:n.*741G>T
NM_000909.6:c.*741G>T MANE Select NP_000900.1:n.*741G>T
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