Canonical Allele Identifier: CA790184447

Gene: NPY1R

Linked Data

• dbSNP Id: rs1261684403
• gnomAD v3: 4-163324703-C-T
• gnomAD v4: 4-163324703-C-T
• MyVariant Identifiers: chr4:g.164245855C>T (hg19) ; chr4:g.163324703C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.163324703C>T , CM000666.2:g.163324703C>T	GRCh38
NC_000004.11:g.164245855C>T , CM000666.1:g.164245855C>T	GRCh37
NC_000004.10:g.164465305C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000296533.3:c.*600G>A MANE Select	ENSP00000354652.2:n.*600G>A
ENST00000296533.2:c.*600G>A	ENSP00000354652.2:n.*600G>A
NM_000909.5:c.*600G>A	NP_000900.1:n.*600G>A
XM_005263031.2:c.*600G>A	XP_005263088.1:n.*600G>A
XM_011532010.1:c.*600G>A	XP_011530312.1:n.*600G>A
XM_005263031.4:c.*600G>A	XP_005263088.1:n.*600G>A
XM_011532010.3:c.*600G>A	XP_011530312.1:n.*600G>A
NM_000909.6:c.*600G>A MANE Select	NP_000900.1:n.*600G>A