Canonical Allele Identifier: CA1058163133

Gene: DYNLT2B TM4SF19-DYNLT2B

Linked Data

• gnomAD v3: 3-196317909-G-GAA
• gnomAD v4: 3-196317909-G-GAA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.196317909_196317910insAA , CM000665.2:g.196317909_196317910insAA	GRCh38
NC_000003.11:g.196044780_196044781insAA , CM000665.1:g.196044780_196044781insAA	GRCh37
NC_000003.10:g.197529177_197529178insAA	NCBI36
NG_054930.1:g.5385_5386insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325318.10:c.113+130_113+131insTT (DYNLT2B) MANE Select	ENSP00000324323.5:n.113+130_113+131insTT
ENST00000325318.9:c.113+130_113+131insTT (DYNLT2B)	ENSP00000324323.5:n.113+130_113+131insTT
ENST00000426563.5:c.117+126_117+127insTT (DYNLT2B)	ENSP00000415835.1:n.117+126_117+127insTT
ENST00000431391.1:c.113+130_113+131insTT	ENSP00000405181.1:n.113+130_113+131insTT
ENST00000442633.1:c.*74-1679_*74-1678insTT (TM4SF19-DYNLT2B)	ENSP00000405973.1:n.*74-1679_*74-1678insTT
ENST00000446494.1:c.113+130_113+131insTT (DYNLT2B)	ENSP00000410605.1:n.113+130_113+131insTT
NM_152773.4:c.113+130_113+131insTT (DYNLT2B)	NP_689986.2:n.113+130_113+131insTT
NR_037950.1:n.862-1679_862-1678insTT (TM4SF19-DYNLT2B)
NM_001351628.1:c.113+130_113+131insTT (DYNLT2B)	NP_001338557.1:n.113+130_113+131insTT
XR_001740547.1:n.96_97insTT
NM_152773.5:c.113+130_113+131insTT (DYNLT2B) MANE Select	NP_689986.2:n.113+130_113+131insTT
NM_001351628.2:c.113+130_113+131insTT (DYNLT2B)	NP_001338557.1:n.113+130_113+131insTT