Canonical Allele Identifier: CA1505231321
Gene: NPY2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.155209808T= , CM000666.2:g.155209808T= GRCh38
NC_000004.11:g.156130960T= , CM000666.1:g.156130960T= GRCh37
NC_000004.10:g.156350410T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000329476.4:c.-49+739T= MANE Select ENSP00000332591.3:n.-49+739T=
ENST00000329476.3:c.-49+739T= ENSP00000332591.3:n.-49+739T=
ENST00000506608.1:c.-49+743T= ENSP00000426366.1:n.-49+743T=
NM_000910.3:c.-49+739T= NP_000901.1:n.-49+739T=
XM_005263033.3:c.-48-4084T= XP_005263090.1:n.-48-4084T=
XM_005263034.3:c.-49+743T= XP_005263091.1:n.-49+743T=
XM_005263033.4:c.-48-4084T= XP_005263090.1:n.-48-4084T=
XM_005263034.4:c.-49+743T= XP_005263091.1:n.-49+743T=
NM_000910.4:c.-49+739T= MANE Select NP_000901.1:n.-49+739T=
NM_001370180.1:c.-49+743T= NP_001357109.1:n.-49+743T=
NM_001375470.1:c.-48-4084T= NP_001362399.1:n.-48-4084T=