Canonical Allele Identifier: CA566955571
Gene: SUPT3H HGNC NCBI

Linked Data

dbSNP Id: rs1158313468

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44810015_44810017del , CM000668.2:g.44810015_44810017del GRCh38
NC_000006.11:g.44777752_44777754del , CM000668.1:g.44777752_44777754del GRCh37
NC_000006.10:g.44885730_44885732del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475057.5:c.*53-513_*53-511del ENSP00000436411.1:n.*53-513_*53-511del
XR_926319.1:n.1091-513_1091-511del
XR_926854.1:n.341-19573_341-19571del
XR_926855.1:n.172-19573_172-19571del
NR_146632.1:n.1104-513_1104-511del
NR_146633.1:n.1166-513_1166-511del
NR_146634.1:n.1118-513_1118-511del
NR_146635.1:n.1163-513_1163-511del
XR_002956310.1:n.1432-513_1432-511del
XR_926319.3:n.1091-513_1091-511del
XR_926854.2:n.365-19573_365-19571del
XR_926855.2:n.246-19573_246-19571del
NR_146632.2:n.1174-513_1174-511del
NR_146634.2:n.1160-513_1160-511del
NR_146635.2:n.1307-513_1307-511del