Canonical Allele Identifier: CA137993235

Gene: SUPT3H

Linked Data

• dbSNP Id: rs776546014
• MyVariant Identifiers: chr6:g.44777808_44777810del (hg19) ; chr6:g.44810071_44810073del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44810073_44810075del , CM000668.2:g.44810073_44810075del	GRCh38
NC_000006.11:g.44777810_44777812del , CM000668.1:g.44777810_44777812del	GRCh37
NC_000006.10:g.44885788_44885790del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475057.5:c.*53-572_*53-570del	ENSP00000436411.1:n.*53-572_*53-570del
XR_926319.1:n.1091-572_1091-570del
XR_926854.1:n.341-19515_341-19513del
XR_926855.1:n.172-19515_172-19513del
NR_146632.1:n.1104-572_1104-570del
NR_146633.1:n.1166-572_1166-570del
NR_146634.1:n.1118-572_1118-570del
NR_146635.1:n.1163-572_1163-570del
XR_002956310.1:n.1432-572_1432-570del
XR_926319.3:n.1091-572_1091-570del
XR_926854.2:n.365-19515_365-19513del
XR_926855.2:n.246-19515_246-19513del
NR_146632.2:n.1174-572_1174-570del
NR_146634.2:n.1160-572_1160-570del
NR_146635.2:n.1307-572_1307-570del