Canonical Allele Identifier: CA1505231340
Gene: NPY2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.155209848T= , CM000666.2:g.155209848T= GRCh38
NC_000004.11:g.156131000T= , CM000666.1:g.156131000T= GRCh37
NC_000004.10:g.156350450T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000329476.4:c.-49+779T= MANE Select ENSP00000332591.3:n.-49+779T=
ENST00000329476.3:c.-49+779T= ENSP00000332591.3:n.-49+779T=
ENST00000506608.1:c.-49+783T= ENSP00000426366.1:n.-49+783T=
NM_000910.3:c.-49+779T= NP_000901.1:n.-49+779T=
XM_005263033.3:c.-48-4044T= XP_005263090.1:n.-48-4044T=
XM_005263034.3:c.-49+783T= XP_005263091.1:n.-49+783T=
XM_005263033.4:c.-48-4044T= XP_005263090.1:n.-48-4044T=
XM_005263034.4:c.-49+783T= XP_005263091.1:n.-49+783T=
NM_000910.4:c.-49+779T= MANE Select NP_000901.1:n.-49+779T=
NM_001370180.1:c.-49+783T= NP_001357109.1:n.-49+783T=
NM_001375470.1:c.-48-4044T= NP_001362399.1:n.-48-4044T=