Canonical Allele Identifier: CA1431592895

Gene: DYNLT2B TM4SF19-DYNLT2B

Linked Data

• dbSNP Id: rs1726930374
• gnomAD v4: 3-196317980-G-GCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.196317982_196317984dup , CM000665.2:g.196317982_196317984dup	GRCh38
NC_000003.11:g.196044853_196044855dup , CM000665.1:g.196044853_196044855dup	GRCh37
NC_000003.10:g.197529250_197529252dup	NCBI36
NG_054930.1:g.5312_5314dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325318.10:c.113+57_113+59dup (DYNLT2B) MANE Select	ENSP00000324323.5:n.113+57_113+59dup
ENST00000325318.9:c.113+57_113+59dup (DYNLT2B)	ENSP00000324323.5:n.113+57_113+59dup
ENST00000426563.5:c.117+53_117+55dup (DYNLT2B)	ENSP00000415835.1:n.117+53_117+55dup
ENST00000431391.1:c.113+57_113+59dup	ENSP00000405181.1:n.113+57_113+59dup
ENST00000442633.1:c.*74-1752_*74-1750dup (TM4SF19-DYNLT2B)	ENSP00000405973.1:n.*74-1752_*74-1750dup
ENST00000446494.1:c.113+57_113+59dup (DYNLT2B)	ENSP00000410605.1:n.113+57_113+59dup
NM_152773.4:c.113+57_113+59dup (DYNLT2B)	NP_689986.2:n.113+57_113+59dup
NR_037950.1:n.862-1752_862-1750dup (TM4SF19-DYNLT2B)
NM_001351628.1:c.113+57_113+59dup (DYNLT2B)	NP_001338557.1:n.113+57_113+59dup
XR_001740547.1:n.23_25dup
NM_152773.5:c.113+57_113+59dup (DYNLT2B) MANE Select	NP_689986.2:n.113+57_113+59dup
NM_001351628.2:c.113+57_113+59dup (DYNLT2B)	NP_001338557.1:n.113+57_113+59dup