Canonical Allele Identifier: CA2576002489
Gene: HERPUD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56935162del , CM000678.2:g.56935162del GRCh38
NC_000016.9:g.56969074del , CM000678.1:g.56969074del GRCh37
NC_000016.8:g.55526575del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439977.7:c.148-73del MANE Select ENSP00000409555.2:n.148-73del
ENST00000300302.9:c.148-73del ENSP00000300302.5:n.148-73del
ENST00000344114.8:c.148-73del ENSP00000340931.4:n.148-73del
ENST00000379792.6:c.148-73del ENSP00000369118.2:n.148-73del
ENST00000439977.6:c.148-73del ENSP00000409555.2:n.148-73del
ENST00000562914.1:n.251-73del
ENST00000563343.5:c.22-73del ENSP00000455094.1:n.22-73del
ENST00000565966.5:c.148-80del ENSP00000456384.1:n.148-80del
ENST00000566550.1:n.198del
ENST00000568676.5:n.246-73del
ENST00000569429.5:c.22-73del ENSP00000457321.1:n.22-73del
ENST00000569569.5:n.246-73del
ENST00000570273.5:n.245-73del
NM_001010989.2:c.148-73del NP_001010989.1:n.148-73del
NM_001272103.1:c.148-73del NP_001259032.1:n.148-73del
NM_014685.3:c.148-73del NP_055500.1:n.148-73del
XM_006721352.2:c.331-73del XP_006721415.1:n.331-73del
NM_014685.4:c.148-73del MANE Select NP_055500.1:n.148-73del
NM_001010989.3:c.148-73del NP_001010989.1:n.148-73del
NM_001272103.2:c.148-73del NP_001259032.1:n.148-73del