Canonical Allele Identifier: CA16616878

Gene: DYNLT2B TM4SF19-DYNLT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.196318038G>C , CM000665.2:g.196318038G>C	GRCh38
NC_000003.11:g.196044909G>C , CM000665.1:g.196044909G>C	GRCh37
NC_000003.10:g.197529306G>C	NCBI36
NG_054930.1:g.5257C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_152773.5:c.113+2C>G (DYNLT2B) MANE Select	NP_689986.2:n.113+2C>G
ENST00000325318.10:c.113+2C>G (DYNLT2B) MANE Select	ENSP00000324323.5:n.113+2C>G
NM_001351628.1:c.113+2C>G (DYNLT2B)	NP_001338557.1:n.113+2C>G
NM_001351628.2:c.113+2C>G (DYNLT2B)	NP_001338557.1:n.113+2C>G
NM_152773.4:c.113+2C>G (DYNLT2B)	NP_689986.2:n.113+2C>G
NR_037950.1:n.862-1807C>G (TM4SF19-DYNLT2B)
ENST00000325318.9:c.113+2C>G (DYNLT2B)	ENSP00000324323.5:n.113+2C>G
ENST00000426563.5:c.115C>G (DYNLT2B)	ENSP00000415835.1:p.Arg39Gly
ENST00000431391.1:c.113+2C>G	ENSP00000405181.1:n.113+2C>G
ENST00000442633.1:c.*74-1807C>G (TM4SF19-DYNLT2B)	ENSP00000405973.1:n.*74-1807C>G
ENST00000446494.1:c.113+2C>G (DYNLT2B)	ENSP00000410605.1:n.113+2C>G