Canonical Allele Identifier: CA2669269675
Gene: DYNLT2B HGNC NCBI
TM4SF19-DYNLT2B HGNC NCBI

Linked Data

gnomAD v4: 3-196317963-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.196317966del , CM000665.2:g.196317966del GRCh38
NC_000003.11:g.196044837del , CM000665.1:g.196044837del GRCh37
NC_000003.10:g.197529234del NCBI36
NG_054930.1:g.5331del

Transcript Alleles

HGVS Amino-acid change
ENST00000325318.10:c.113+76del (DYNLT2B) MANE Select ENSP00000324323.5:n.113+76del
ENST00000325318.9:c.113+76del (DYNLT2B) ENSP00000324323.5:n.113+76del
ENST00000426563.5:c.117+72del (DYNLT2B) ENSP00000415835.1:n.117+72del
ENST00000431391.1:c.113+76del ENSP00000405181.1:n.113+76del
ENST00000442633.1:c.*74-1733del (TM4SF19-DYNLT2B) ENSP00000405973.1:n.*74-1733del
ENST00000446494.1:c.113+76del (DYNLT2B) ENSP00000410605.1:n.113+76del
NM_152773.4:c.113+76del (DYNLT2B) NP_689986.2:n.113+76del
NR_037950.1:n.862-1733del (TM4SF19-DYNLT2B)
NM_001351628.1:c.113+76del (DYNLT2B) NP_001338557.1:n.113+76del
XR_001740547.1:n.42del
NM_152773.5:c.113+76del (DYNLT2B) MANE Select NP_689986.2:n.113+76del
NM_001351628.2:c.113+76del (DYNLT2B) NP_001338557.1:n.113+76del
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