Canonical Allele Identifier: CA2581400186
Gene: NPY1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324599G>C , CM000666.2:g.163324599G>C GRCh38
NC_000004.11:g.164245751G>C , CM000666.1:g.164245751G>C GRCh37
NC_000004.10:g.164465201G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296533.3:c.*704C>G MANE Select ENSP00000354652.2:n.*704C>G
ENST00000296533.2:c.*704C>G ENSP00000354652.2:n.*704C>G
NM_000909.5:c.*704C>G NP_000900.1:n.*704C>G
XM_005263031.2:c.*704C>G XP_005263088.1:n.*704C>G
XM_011532010.1:c.*704C>G XP_011530312.1:n.*704C>G
XM_005263031.4:c.*704C>G XP_005263088.1:n.*704C>G
XM_011532010.3:c.*704C>G XP_011530312.1:n.*704C>G
NM_000909.6:c.*704C>G MANE Select NP_000900.1:n.*704C>G