Canonical Allele Identifier: CA2515481436
Gene: NPY1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324593A>G , CM000666.2:g.163324593A>G GRCh38
NC_000004.11:g.164245745A>G , CM000666.1:g.164245745A>G GRCh37
NC_000004.10:g.164465195A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296533.3:c.*710T>C MANE Select ENSP00000354652.2:n.*710T>C
ENST00000296533.2:c.*710T>C ENSP00000354652.2:n.*710T>C
NM_000909.5:c.*710T>C NP_000900.1:n.*710T>C
XM_005263031.2:c.*710T>C XP_005263088.1:n.*710T>C
XM_011532010.1:c.*710T>C XP_011530312.1:n.*710T>C
XM_005263031.4:c.*710T>C XP_005263088.1:n.*710T>C
XM_011532010.3:c.*710T>C XP_011530312.1:n.*710T>C
NM_000909.6:c.*710T>C MANE Select NP_000900.1:n.*710T>C