Canonical Allele Identifier: CA2672548348

Gene: NPY1R

Linked Data

• gnomAD v4: 4-163324788-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.163324788A>G , CM000666.2:g.163324788A>G	GRCh38
NC_000004.11:g.164245940A>G , CM000666.1:g.164245940A>G	GRCh37
NC_000004.10:g.164465390A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296533.3:c.*515T>C MANE Select	ENSP00000354652.2:n.*515T>C
ENST00000296533.2:c.*515T>C	ENSP00000354652.2:n.*515T>C
NM_000909.5:c.*515T>C	NP_000900.1:n.*515T>C
XM_005263031.2:c.*515T>C	XP_005263088.1:n.*515T>C
XM_011532010.1:c.*515T>C	XP_011530312.1:n.*515T>C
XM_005263031.4:c.*515T>C	XP_005263088.1:n.*515T>C
XM_011532010.3:c.*515T>C	XP_011530312.1:n.*515T>C
NM_000909.6:c.*515T>C MANE Select	NP_000900.1:n.*515T>C