Canonical Allele Identifier: CA1474790390

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88523703T= , CM000666.2:g.88523703T= GRCh38
NC_000004.11:g.89444854T= , CM000666.1:g.89444854T= GRCh37
NC_000004.10:g.89663877T= NCBI36
NG_046719.1:g.5099A=

Transcript Alleles

HGVS Amino-acid change
ENST00000273968.5:c.-3A= (PYURF) MANE Select ENSP00000273968.4:n.-3A=
ENST00000527353.2:c.-446A= (PIGY) MANE Select ENSP00000432688.1:n.-446A=
ENST00000273968.4:c.-3A= (PYURF) ENSP00000273968.4:n.-3A=
ENST00000601319.1:n.1188T= (HERC3)
NM_001042616.2:c.-446A= (PIGY) NP_001036081.1:n.-446A=
NM_032906.4:c.-3A= (PYURF) NP_116295.1:n.-3A=
NM_032906.5:c.-3A= (PYURF) MANE Select NP_116295.1:n.-3A=
NM_001042616.3:c.-446A= (PIGY) MANE Select NP_001036081.1:n.-446A=