Canonical Allele Identifier: CA1656226946
Gene: HS3ST5 HGNC NCBI
HDAC2-AS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.114301207_114301210delinsAAGC , CM000668.2:g.114301207_114301210delinsAAGC GRCh38
NC_000006.11:g.114622371_114622374delinsAAGC , CM000668.1:g.114622371_114622374delinsAAGC GRCh37
NC_000006.10:g.114729064_114729067delinsAAGC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000312719.10:c.-339+40985_-339+40988delinsGCTT (HS3ST5) MANE Select ENSP00000427888.1:n.-339+40985_-339+40988delinsGCTT
ENST00000312719.9:c.-339+40985_-339+40988delinsGCTT (HS3ST5) ENSP00000427888.1:n.-339+40985_-339+40988delinsGCTT
NR_125845.1:n.1800-39315_1800-39312delinsAAGC (HDAC2-AS2)
XM_006715379.2:c.-339+40985_-339+40988delinsGCTT (HS3ST5) XP_006715442.1:n.-339+40985_-339+40988delinsGCTT
XM_011535587.1:c.-339+40162_-339+40165delinsGCTT (HS3ST5) XP_011533889.1:n.-339+40162_-339+40165delinsGCTT
XR_942347.1:n.239+40985_239+40988delinsGCTT (HS3ST5)
XM_017010470.1:c.-339+40162_-339+40165delinsGCTT (HS3ST5) XP_016865959.1:n.-339+40162_-339+40165delinsGCTT
XM_017010473.1:c.-335+40162_-335+40165delinsGCTT (HS3ST5) XP_016865962.1:n.-335+40162_-335+40165delinsGCTT
XM_017010474.2:c.-335+40985_-335+40988delinsGCTT (HS3ST5) XP_016865963.1:n.-335+40985_-335+40988delinsGCTT
NM_001387039.1:c.-227+40162_-227+40165delinsGCTT (HS3ST5) NP_001373968.1:n.-227+40162_-227+40165delinsGCTT
NM_001387040.1:c.-33+40985_-33+40988delinsGCTT (HS3ST5) NP_001373969.1:n.-33+40985_-33+40988delinsGCTT
NM_001387041.1:c.-335+40985_-335+40988delinsGCTT (HS3ST5) NP_001373970.1:n.-335+40985_-335+40988delinsGCTT
NM_001387042.1:c.-339+40162_-339+40165delinsGCTT (HS3ST5) NP_001373971.1:n.-339+40162_-339+40165delinsGCTT
NM_001387043.1:c.-335+40162_-335+40165delinsGCTT (HS3ST5) NP_001373972.1:n.-335+40162_-335+40165delinsGCTT
NM_001387044.1:c.-429+40985_-429+40988delinsGCTT (HS3ST5) NP_001373973.1:n.-429+40985_-429+40988delinsGCTT
NM_001387045.1:c.-434+40985_-434+40988delinsGCTT (HS3ST5) NP_001373974.1:n.-434+40985_-434+40988delinsGCTT
NM_001387046.1:c.-227+40985_-227+40988delinsGCTT (HS3ST5) NP_001373975.1:n.-227+40985_-227+40988delinsGCTT
NM_001387047.1:c.-434+40162_-434+40165delinsGCTT (HS3ST5) NP_001373976.1:n.-434+40162_-434+40165delinsGCTT
NM_153612.4:c.-339+40985_-339+40988delinsGCTT (HS3ST5) MANE Select NP_705840.2:n.-339+40985_-339+40988delinsGCTT
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