Canonical Allele Identifier: CA2261156792
Gene: PYY HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43953035C= , CM000679.2:g.43953035C= GRCh38
NC_000017.10:g.42030403C= , CM000679.1:g.42030403C= GRCh37
NC_000017.9:g.39385929C= NCBI36
NG_023338.1:g.56435G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.*70G= ENSP00000467310.1:n.*70G=
ENST00000692052.1:c.270-55G= MANE Select ENSP00000509262.1:n.270-55G=
ENST00000360085.6:c.270-55G= ENSP00000353198.1:n.270-55G=
ENST00000592796.1:c.*70G= ENSP00000467310.1:n.*70G=
NM_004160.4:c.270-55G= NP_004151.3:n.270-55G=
XM_011525035.1:c.270-55G= XP_011523337.1:n.270-55G=
NM_004160.5:c.270-55G= NP_004151.3:n.270-55G=
NM_001394028.1:c.270-55G= MANE Select NP_001380957.1:n.270-55G=
NM_001394029.1:c.*70G= NP_001380958.1:n.*70G=
NM_004160.6:c.270-55G= NP_004151.4:n.270-55G=
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