Canonical Allele Identifier: CA2224380098
Gene: HERPUD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56935172_56935174delinsCTG , CM000678.2:g.56935172_56935174delinsCTG GRCh38
NC_000016.9:g.56969084_56969086delinsCTG , CM000678.1:g.56969084_56969086delinsCTG GRCh37
NC_000016.8:g.55526585_55526587delinsCTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439977.7:c.148-63_148-61delinsCTG MANE Select ENSP00000409555.2:n.148-63_148-61delinsCTG
ENST00000300302.9:c.148-63_148-61delinsCTG ENSP00000300302.5:n.148-63_148-61delinsCTG
ENST00000344114.8:c.148-63_148-61delinsCTG ENSP00000340931.4:n.148-63_148-61delinsCTG
ENST00000379792.6:c.148-63_148-61delinsCTG ENSP00000369118.2:n.148-63_148-61delinsCTG
ENST00000439977.6:c.148-63_148-61delinsCTG ENSP00000409555.2:n.148-63_148-61delinsCTG
ENST00000562914.1:n.251-63_251-61delinsCTG
ENST00000563343.5:c.22-63_22-61delinsCTG ENSP00000455094.1:n.22-63_22-61delinsCTG
ENST00000565966.5:c.148-70_148-68delinsCTG ENSP00000456384.1:n.148-70_148-68delinsCTG
ENST00000566550.1:n.208_210delinsCTG
ENST00000568676.5:n.246-63_246-61delinsCTG
ENST00000569429.5:c.22-63_22-61delinsCTG ENSP00000457321.1:n.22-63_22-61delinsCTG
ENST00000569569.5:n.246-63_246-61delinsCTG
ENST00000570273.5:n.245-63_245-61delinsCTG
NM_001010989.2:c.148-63_148-61delinsCTG NP_001010989.1:n.148-63_148-61delinsCTG
NM_001272103.1:c.148-63_148-61delinsCTG NP_001259032.1:n.148-63_148-61delinsCTG
NM_014685.3:c.148-63_148-61delinsCTG NP_055500.1:n.148-63_148-61delinsCTG
XM_006721352.2:c.331-63_331-61delinsCTG XP_006721415.1:n.331-63_331-61delinsCTG
NM_014685.4:c.148-63_148-61delinsCTG MANE Select NP_055500.1:n.148-63_148-61delinsCTG
NM_001010989.3:c.148-63_148-61delinsCTG NP_001010989.1:n.148-63_148-61delinsCTG
NM_001272103.2:c.148-63_148-61delinsCTG NP_001259032.1:n.148-63_148-61delinsCTG