Canonical Allele Identifier: CA1140038829

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159001296A= , CM000663.2:g.159001296A= GRCh38
NC_000001.10:g.158971086A= , CM000663.1:g.158971086A= GRCh37
NC_000001.9:g.157237710A= NCBI36
NG_029141.2:g.6327A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696987.1:c.-984T= (PYDC5) MANE Select ENSP00000513023.1:n.-984T=
ENST00000566111.5:c.-180+901A= (IFI16) ENSP00000458084.1:n.-180+901A=
XM_005245127.2:c.-168+901A= (IFI16) XP_005245184.1:n.-168+901A=
NM_001364867.1:c.-180+901A= (IFI16) NP_001351796.1:n.-180+901A=
XM_017001149.2:c.-168+901A= (IFI16) XP_016856638.1:n.-168+901A=
XR_001737000.1:n.1708-8707A= (PYHIN1)
XR_001737001.1:n.2051-8707A= (PYHIN1)
XR_001737002.1:n.1574-8707A= (PYHIN1)
NM_001364867.2:c.-180+901A= (IFI16) NP_001351796.1:n.-180+901A=
NM_001376588.1:c.-180+901A= (IFI16) NP_001363517.1:n.-180+901A=
NM_001376591.1:c.-180+901A= (IFI16) NP_001363520.1:n.-180+901A=
NM_001320010.2:c.-984T= (PYDC5) MANE Select NP_001306939.1:n.-984T=