Canonical Allele Identifier: CA357643946

Linked Data

gnomAD v4: 4-88523698-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88523698C>T , CM000666.2:g.88523698C>T GRCh38
NC_000004.11:g.89444849C>T , CM000666.1:g.89444849C>T GRCh37
NC_000004.10:g.89663872C>T NCBI36
NG_046719.1:g.5104G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000273968.5:c.3G>A (PYURF) MANE Select ENSP00000273968.4:p.Met1Ile
ENST00000527353.2:c.-441G>A (PIGY) MANE Select ENSP00000432688.1:n.-441G>A
ENST00000273968.4:c.3G>A (PYURF) ENSP00000273968.4:p.Met1Ile
ENST00000601319.1:n.1183C>T (HERC3)
NM_001042616.2:c.-441G>A (PIGY) NP_001036081.1:n.-441G>A
NM_032906.4:c.3G>A (PYURF) NP_116295.1:p.Met1Ile
NM_032906.5:c.3G>A (PYURF) MANE Select NP_116295.1:p.Met1Ile
NM_001042616.3:c.-441G>A (PIGY) MANE Select NP_001036081.1:n.-441G>A