Canonical Allele Identifier: CA1474790396

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88523708C= , CM000666.2:g.88523708C= GRCh38
NC_000004.11:g.89444859C= , CM000666.1:g.89444859C= GRCh37
NC_000004.10:g.89663882C= NCBI36
NG_046719.1:g.5094G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000273968.5:c.-8G= (PYURF) MANE Select ENSP00000273968.4:n.-8G=
ENST00000527353.2:c.-451G= (PIGY) MANE Select ENSP00000432688.1:n.-451G=
ENST00000273968.4:c.-8G= (PYURF) ENSP00000273968.4:n.-8G=
ENST00000601319.1:n.1193C= (HERC3)
NM_001042616.2:c.-451G= (PIGY) NP_001036081.1:n.-451G=
NM_032906.4:c.-8G= (PYURF) NP_116295.1:n.-8G=
NM_032906.5:c.-8G= (PYURF) MANE Select NP_116295.1:n.-8G=
NM_001042616.3:c.-451G= (PIGY) MANE Select NP_001036081.1:n.-451G=