Canonical Allele Identifier: CA2493908448

Gene: DYNC2LI1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43774140T= , CM000664.2:g.43774140T=	GRCh38
NC_000002.11:g.44001279T= , CM000664.1:g.44001279T=	GRCh37
NC_000002.10:g.43854783T=	NCBI36
NG_053008.1:g.5102T=

Transcript Alleles

HGVS	Amino-acid Change
NM_016008.4:c.2T= MANE Select	NP_057092.2:p.Met1=
ENST00000260605.12:c.2T= MANE Select	ENSP00000260605.8:p.Met1=
NM_001193464.1:c.2T=	NP_001180393.1:p.Met1=
NM_001193464.2:c.2T=	NP_001180393.1:p.Met1=
NM_001348912.1:c.2T=	NP_001335841.1:p.Met1=
NM_001348912.2:c.2T=	NP_001335841.1:p.Met1=
NM_001348913.1:c.2T=	NP_001335842.1:p.Met1=
NM_001348913.2:c.2T=	NP_001335842.1:p.Met1=
NM_015522.3:c.2T=	NP_056337.1:p.Met1=
NM_015522.4:c.2T=	NP_056337.1:p.Met1=
NM_016008.3:c.2T=	NP_057092.2:p.Met1=
ENST00000398823.6:c.2T=	ENSP00000381804.2:p.Met1=
ENST00000406852.7:c.2T=	ENSP00000385738.3:p.Met1=
ENST00000462426.1:c.2T=	ENSP00000428082.1:p.Met1=
ENST00000479242.5:c.2T=	ENSP00000430525.1:p.Met1=
ENST00000489222.6:n.77T=
ENST00000496980.6:c.2T=	ENSP00000430356.1:p.Met1=
ENST00000605786.5:c.2T=	ENSP00000474032.1:p.Met1=
XM_005264364.3:c.2T=	XP_005264421.1:p.Met1=
XM_005264365.3:c.2T=	XP_005264422.1:p.Met1=