Canonical Allele Identifier: CA1505231324
Gene: NPY2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.155209811_155209813delinsGAT , CM000666.2:g.155209811_155209813delinsGAT GRCh38
NC_000004.11:g.156130963_156130965delinsGAT , CM000666.1:g.156130963_156130965delinsGAT GRCh37
NC_000004.10:g.156350413_156350415delinsGAT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000329476.4:c.-49+742_-49+744delinsGAT MANE Select ENSP00000332591.3:n.-49+742_-49+744delins...
ENST00000329476.3:c.-49+742_-49+744delinsGAT ENSP00000332591.3:n.-49+742_-49+744delins...
ENST00000506608.1:c.-49+746_-49+748delinsGAT ENSP00000426366.1:n.-49+746_-49+748delins...
NM_000910.3:c.-49+742_-49+744delinsGAT NP_000901.1:n.-49+742_-49+744delinsGAT
XM_005263033.3:c.-48-4081_-48-4079delinsGAT XP_005263090.1:n.-48-4081_-48-4079delinsG...
XM_005263034.3:c.-49+746_-49+748delinsGAT XP_005263091.1:n.-49+746_-49+748delinsGAT...
XM_005263033.4:c.-48-4081_-48-4079delinsGAT XP_005263090.1:n.-48-4081_-48-4079delinsG...
XM_005263034.4:c.-49+746_-49+748delinsGAT XP_005263091.1:n.-49+746_-49+748delinsGAT...
NM_000910.4:c.-49+742_-49+744delinsGAT MANE Select NP_000901.1:n.-49+742_-49+744delinsGAT
NM_001370180.1:c.-49+746_-49+748delinsGAT NP_001357109.1:n.-49+746_-49+748delinsGAT...
NM_001375470.1:c.-48-4081_-48-4079delinsGAT NP_001362399.1:n.-48-4081_-48-4079delinsG...