Canonical Allele Identifier: CA357643952

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88523700T>A , CM000666.2:g.88523700T>A GRCh38
NC_000004.11:g.89444851T>A , CM000666.1:g.89444851T>A GRCh37
NC_000004.10:g.89663874T>A NCBI36
NG_046719.1:g.5102A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000273968.5:c.1A>T (PYURF) MANE Select ENSP00000273968.4:p.Met1Leu
ENST00000527353.2:c.-443A>T (PIGY) MANE Select ENSP00000432688.1:n.-443A>T
ENST00000273968.4:c.1A>T (PYURF) ENSP00000273968.4:p.Met1Leu
ENST00000601319.1:n.1185T>A (HERC3)
NM_001042616.2:c.-443A>T (PIGY) NP_001036081.1:n.-443A>T
NM_032906.4:c.1A>T (PYURF) NP_116295.1:p.Met1Leu
NM_032906.5:c.1A>T (PYURF) MANE Select NP_116295.1:p.Met1Leu
NM_001042616.3:c.-443A>T (PIGY) MANE Select NP_001036081.1:n.-443A>T