Canonical Allele Identifier: CA626222525

Gene: PYY

Linked Data

• dbSNP Id: rs1248250968
• gnomAD v2: 17-42030461-TA-T
• gnomAD v4: 17-43953093-TA-T
• MyVariant Identifiers: chr17:g.42030462del (hg19) ; chr17:g.43953094del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43953095del , CM000679.2:g.43953095del	GRCh38
NC_000017.10:g.42030463del , CM000679.1:g.42030463del	GRCh37
NC_000017.9:g.39385989del	NCBI36
NG_023338.1:g.56376del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*11del	ENSP00000467310.1:n.*11del
ENST00000692052.1:c.269+15del MANE Select	ENSP00000509262.1:n.269+15del
ENST00000360085.6:c.269+15del	ENSP00000353198.1:n.269+15del
ENST00000592796.1:c.*11del	ENSP00000467310.1:n.*11del
NM_004160.4:c.269+15del	NP_004151.3:n.269+15del
XM_011525035.1:c.269+15del	XP_011523337.1:n.269+15del
NM_004160.5:c.269+15del	NP_004151.3:n.269+15del
NM_001394028.1:c.269+15del MANE Select	NP_001380957.1:n.269+15del
NM_001394029.1:c.*11del	NP_001380958.1:n.*11del
NM_004160.6:c.269+15del	NP_004151.4:n.269+15del