Canonical Allele Identifier: CA1625150251
Gene: SUPT3H HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44810070_44810073delinsACTT , CM000668.2:g.44810070_44810073delinsACTT GRCh38
NC_000006.11:g.44777807_44777810delinsACTT , CM000668.1:g.44777807_44777810delinsACTT GRCh37
NC_000006.10:g.44885785_44885788delinsACTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475057.5:c.*53-572_*53-569delinsAAGT ENSP00000436411.1:n.*53-572_*53-569delinsAAGT
XR_926319.1:n.1091-572_1091-569delinsAAGT
XR_926854.1:n.341-19518_341-19515delinsACTT
XR_926855.1:n.172-19518_172-19515delinsACTT
NR_146632.1:n.1104-572_1104-569delinsAAGT
NR_146633.1:n.1166-572_1166-569delinsAAGT
NR_146634.1:n.1118-572_1118-569delinsAAGT
NR_146635.1:n.1163-572_1163-569delinsAAGT
XR_002956310.1:n.1432-572_1432-569delinsAAGT
XR_926319.3:n.1091-572_1091-569delinsAAGT
XR_926854.2:n.365-19518_365-19515delinsACTT
XR_926855.2:n.246-19518_246-19515delinsACTT
NR_146632.2:n.1174-572_1174-569delinsAAGT
NR_146634.2:n.1160-572_1160-569delinsAAGT
NR_146635.2:n.1307-572_1307-569delinsAAGT