Canonical Allele Identifier: CA1656226975

Gene: HS3ST5 HDAC2-AS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.114301265_114301266delinsAT , CM000668.2:g.114301265_114301266delinsAT	GRCh38
NC_000006.11:g.114622429_114622430delinsAT , CM000668.1:g.114622429_114622430delinsAT	GRCh37
NC_000006.10:g.114729122_114729123delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312719.10:c.-339+40929_-339+40930delinsAT (HS3ST5) MANE Select	ENSP00000427888.1:n.-339+40929_-339+40930delinsAT
ENST00000312719.9:c.-339+40929_-339+40930delinsAT (HS3ST5)	ENSP00000427888.1:n.-339+40929_-339+40930delinsAT
NR_125845.1:n.1800-39257_1800-39256delinsAT (HDAC2-AS2)
XM_006715379.2:c.-339+40929_-339+40930delinsAT (HS3ST5)	XP_006715442.1:n.-339+40929_-339+40930delinsAT
XM_011535587.1:c.-339+40106_-339+40107delinsAT (HS3ST5)	XP_011533889.1:n.-339+40106_-339+40107delinsAT
XR_942347.1:n.239+40929_239+40930delinsAT (HS3ST5)
XM_017010470.1:c.-339+40106_-339+40107delinsAT (HS3ST5)	XP_016865959.1:n.-339+40106_-339+40107delinsAT
XM_017010473.1:c.-335+40106_-335+40107delinsAT (HS3ST5)	XP_016865962.1:n.-335+40106_-335+40107delinsAT
XM_017010474.2:c.-335+40929_-335+40930delinsAT (HS3ST5)	XP_016865963.1:n.-335+40929_-335+40930delinsAT
NM_001387039.1:c.-227+40106_-227+40107delinsAT (HS3ST5)	NP_001373968.1:n.-227+40106_-227+40107delinsAT
NM_001387040.1:c.-33+40929_-33+40930delinsAT (HS3ST5)	NP_001373969.1:n.-33+40929_-33+40930delinsAT
NM_001387041.1:c.-335+40929_-335+40930delinsAT (HS3ST5)	NP_001373970.1:n.-335+40929_-335+40930delinsAT
NM_001387042.1:c.-339+40106_-339+40107delinsAT (HS3ST5)	NP_001373971.1:n.-339+40106_-339+40107delinsAT
NM_001387043.1:c.-335+40106_-335+40107delinsAT (HS3ST5)	NP_001373972.1:n.-335+40106_-335+40107delinsAT
NM_001387044.1:c.-429+40929_-429+40930delinsAT (HS3ST5)	NP_001373973.1:n.-429+40929_-429+40930delinsAT
NM_001387045.1:c.-434+40929_-434+40930delinsAT (HS3ST5)	NP_001373974.1:n.-434+40929_-434+40930delinsAT
NM_001387046.1:c.-227+40929_-227+40930delinsAT (HS3ST5)	NP_001373975.1:n.-227+40929_-227+40930delinsAT
NM_001387047.1:c.-434+40106_-434+40107delinsAT (HS3ST5)	NP_001373976.1:n.-434+40106_-434+40107delinsAT
NM_153612.4:c.-339+40929_-339+40930delinsAT (HS3ST5) MANE Select	NP_705840.2:n.-339+40929_-339+40930delinsAT