Canonical Allele Identifier: CA790184450

Gene: NPY1R

Linked Data

• dbSNP Id: rs1189016320
• gnomAD v3: 4-163324707-C-G
• gnomAD v4: 4-163324707-C-G
• MyVariant Identifiers: chr4:g.164245859C>G (hg19) ; chr4:g.163324707C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.163324707C>G , CM000666.2:g.163324707C>G	GRCh38
NC_000004.11:g.164245859C>G , CM000666.1:g.164245859C>G	GRCh37
NC_000004.10:g.164465309C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000296533.3:c.*596G>C MANE Select	ENSP00000354652.2:n.*596G>C
ENST00000296533.2:c.*596G>C	ENSP00000354652.2:n.*596G>C
NM_000909.5:c.*596G>C	NP_000900.1:n.*596G>C
XM_005263031.2:c.*596G>C	XP_005263088.1:n.*596G>C
XM_011532010.1:c.*596G>C	XP_011530312.1:n.*596G>C
XM_005263031.4:c.*596G>C	XP_005263088.1:n.*596G>C
XM_011532010.3:c.*596G>C	XP_011530312.1:n.*596G>C
NM_000909.6:c.*596G>C MANE Select	NP_000900.1:n.*596G>C