Canonical Allele Identifier: CA1088484179
Gene: SUPT3H HGNC NCBI

Linked Data

dbSNP Id: rs1766386088

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44809767_44809770del , CM000668.2:g.44809767_44809770del GRCh38
NC_000006.11:g.44777504_44777507del , CM000668.1:g.44777504_44777507del GRCh37
NC_000006.10:g.44885482_44885485del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475057.5:c.*53-266_*53-263del ENSP00000436411.1:n.*53-266_*53-263del
XR_926319.1:n.1091-266_1091-263del
XR_926854.1:n.341-19821_341-19818del
XR_926855.1:n.172-19821_172-19818del
NR_146632.1:n.1104-266_1104-263del
NR_146633.1:n.1166-266_1166-263del
NR_146634.1:n.1118-266_1118-263del
NR_146635.1:n.1163-266_1163-263del
XR_002956310.1:n.1432-266_1432-263del
XR_926319.3:n.1091-266_1091-263del
XR_926854.2:n.365-19821_365-19818del
XR_926855.2:n.246-19821_246-19818del
NR_146632.2:n.1174-266_1174-263del
NR_146634.2:n.1160-266_1160-263del
NR_146635.2:n.1307-266_1307-263del