Canonical Allele Identifier: CA1656226916
Gene: HS3ST5 HGNC NCBI
HDAC2-AS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.114301111_114301113delinsCTG , CM000668.2:g.114301111_114301113delinsCTG GRCh38
NC_000006.11:g.114622275_114622277delinsCTG , CM000668.1:g.114622275_114622277delinsCTG GRCh37
NC_000006.10:g.114728968_114728970delinsCTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000312719.10:c.-339+41082_-339+41084delinsCAG (HS3ST5) MANE Select ENSP00000427888.1:n.-339+41082_-339+41084delinsCAG
ENST00000312719.9:c.-339+41082_-339+41084delinsCAG (HS3ST5) ENSP00000427888.1:n.-339+41082_-339+41084delinsCAG
NR_125845.1:n.1800-39411_1800-39409delinsCTG (HDAC2-AS2)
XM_006715379.2:c.-339+41082_-339+41084delinsCAG (HS3ST5) XP_006715442.1:n.-339+41082_-339+41084delinsCAG
XM_011535587.1:c.-339+40259_-339+40261delinsCAG (HS3ST5) XP_011533889.1:n.-339+40259_-339+40261delinsCAG
XR_942347.1:n.239+41082_239+41084delinsCAG (HS3ST5)
XM_017010470.1:c.-339+40259_-339+40261delinsCAG (HS3ST5) XP_016865959.1:n.-339+40259_-339+40261delinsCAG
XM_017010473.1:c.-335+40259_-335+40261delinsCAG (HS3ST5) XP_016865962.1:n.-335+40259_-335+40261delinsCAG
XM_017010474.2:c.-335+41082_-335+41084delinsCAG (HS3ST5) XP_016865963.1:n.-335+41082_-335+41084delinsCAG
NM_001387039.1:c.-227+40259_-227+40261delinsCAG (HS3ST5) NP_001373968.1:n.-227+40259_-227+40261delinsCAG
NM_001387040.1:c.-33+41082_-33+41084delinsCAG (HS3ST5) NP_001373969.1:n.-33+41082_-33+41084delinsCAG
NM_001387041.1:c.-335+41082_-335+41084delinsCAG (HS3ST5) NP_001373970.1:n.-335+41082_-335+41084delinsCAG
NM_001387042.1:c.-339+40259_-339+40261delinsCAG (HS3ST5) NP_001373971.1:n.-339+40259_-339+40261delinsCAG
NM_001387043.1:c.-335+40259_-335+40261delinsCAG (HS3ST5) NP_001373972.1:n.-335+40259_-335+40261delinsCAG
NM_001387044.1:c.-429+41082_-429+41084delinsCAG (HS3ST5) NP_001373973.1:n.-429+41082_-429+41084delinsCAG
NM_001387045.1:c.-434+41082_-434+41084delinsCAG (HS3ST5) NP_001373974.1:n.-434+41082_-434+41084delinsCAG
NM_001387046.1:c.-227+41082_-227+41084delinsCAG (HS3ST5) NP_001373975.1:n.-227+41082_-227+41084delinsCAG
NM_001387047.1:c.-434+40259_-434+40261delinsCAG (HS3ST5) NP_001373976.1:n.-434+40259_-434+40261delinsCAG
NM_153612.4:c.-339+41082_-339+41084delinsCAG (HS3ST5) MANE Select NP_705840.2:n.-339+41082_-339+41084delinsCAG