Canonical Allele Identifier: CA2638142785

Gene: PYY

Linked Data

• gnomAD v4: 17-43952810-G-GAAGGGAAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43952810_43952811insAAGGGAAGA , CM000679.2:g.43952810_43952811insAAGGGAAGA	GRCh38
NC_000017.10:g.42030178_42030179insAAGGGAAGA , CM000679.1:g.42030178_42030179insAAGGGAAGA	GRCh37
NC_000017.9:g.39385704_39385705insAAGGGAAGA	NCBI36
NG_023338.1:g.56659_56660insTCTTCCCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000592796.2:c.*294_*295insTCTTCCCTT	ENSP00000467310.1:n.*294_*295insTCTTCCCTT
ENST00000692052.1:c.*145_*146insTCTTCCCTT MANE Select	ENSP00000509262.1:n.*145_*146insTCTTCCCTT
ENST00000360085.6:c.*145_*146insTCTTCCCTT	ENSP00000353198.1:n.*145_*146insTCTTCCCTT
NM_004160.4:c.*145_*146insTCTTCCCTT	NP_004151.3:n.*145_*146insTCTTCCCTT
XM_011525035.1:c.*145_*146insTCTTCCCTT	XP_011523337.1:n.*145_*146insTCTTCCCTT
NM_004160.5:c.*145_*146insTCTTCCCTT	NP_004151.3:n.*145_*146insTCTTCCCTT
NM_001394028.1:c.*145_*146insTCTTCCCTT MANE Select	NP_001380957.1:n.*145_*146insTCTTCCCTT
NM_001394029.1:c.*294_*295insTCTTCCCTT	NP_001380958.1:n.*294_*295insTCTTCCCTT
NM_004160.6:c.*145_*146insTCTTCCCTT	NP_004151.4:n.*145_*146insTCTTCCCTT