Canonical Allele Identifier: CA1431592872
Gene: DYNLT2B HGNC NCBI
TM4SF19-DYNLT2B HGNC NCBI

Linked Data

dbSNP Id: rs1726927759
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.196317952_196317962del , CM000665.2:g.196317952_196317962del GRCh38
NC_000003.11:g.196044823_196044833del , CM000665.1:g.196044823_196044833del GRCh37
NC_000003.10:g.197529220_197529230del NCBI36
NG_054930.1:g.5334_5344del

Transcript Alleles

HGVS Amino-acid change
ENST00000325318.10:c.113+79_113+89del (DYNLT2B) MANE Select ENSP00000324323.5:n.113+79_113+89del
ENST00000325318.9:c.113+79_113+89del (DYNLT2B) ENSP00000324323.5:n.113+79_113+89del
ENST00000426563.5:c.117+75_117+85del (DYNLT2B) ENSP00000415835.1:n.117+75_117+85del
ENST00000431391.1:c.113+79_113+89del ENSP00000405181.1:n.113+79_113+89del
ENST00000442633.1:c.*74-1730_*74-1720del (TM4SF19-DYNLT2B) ENSP00000405973.1:n.*74-1730_*74-1720del
ENST00000446494.1:c.113+79_113+89del (DYNLT2B) ENSP00000410605.1:n.113+79_113+89del
NM_152773.4:c.113+79_113+89del (DYNLT2B) NP_689986.2:n.113+79_113+89del
NR_037950.1:n.862-1730_862-1720del (TM4SF19-DYNLT2B)
NM_001351628.1:c.113+79_113+89del (DYNLT2B) NP_001338557.1:n.113+79_113+89del
XR_001740547.1:n.45_55del
NM_152773.5:c.113+79_113+89del (DYNLT2B) MANE Select NP_689986.2:n.113+79_113+89del
NM_001351628.2:c.113+79_113+89del (DYNLT2B) NP_001338557.1:n.113+79_113+89del
Search 100 bp 5'
Search 100 bp 3'