Canonical Allele Identifier: CA790184388

Gene: NPY1R

Linked Data

• dbSNP Id: rs1241536503
• gnomAD v3: 4-163324530-ATTTAC-A
• gnomAD v4: 4-163324530-ATTTAC-A
• MyVariant Identifiers: chr4:g.164245683_164245687del (hg19) ; chr4:g.163324531_163324535del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.163324535_163324539del , CM000666.2:g.163324535_163324539del	GRCh38
NC_000004.11:g.164245687_164245691del , CM000666.1:g.164245687_164245691del	GRCh37
NC_000004.10:g.164465137_164465141del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296533.3:c.*768_*772del MANE Select	ENSP00000354652.2:n.*768_*772del
ENST00000296533.2:c.*768_*772del	ENSP00000354652.2:n.*768_*772del
NM_000909.5:c.*768_*772del	NP_000900.1:n.*768_*772del
XM_005263031.2:c.*768_*772del	XP_005263088.1:n.*768_*772del
XM_011532010.1:c.*768_*772del	XP_011530312.1:n.*768_*772del
XM_005263031.4:c.*768_*772del	XP_005263088.1:n.*768_*772del
XM_011532010.3:c.*768_*772del	XP_011530312.1:n.*768_*772del
NM_000909.6:c.*768_*772del MANE Select	NP_000900.1:n.*768_*772del