Canonical Allele Identifier: CA9458081

Gene: AXL

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41237956G= , CM000681.2:g.41237956G=	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
NM_021913.5:c.796G= MANE Select	NP_068713.2:p.Asp266=
ENST00000301178.9:c.796G= MANE Select	ENSP00000301178.3:p.Asp266=
NM_001278599.1:c.-9G=	NP_001265528.1:n.-9G=
NM_001278599.2:c.-9G=	NP_001265528.1:n.-9G=
NM_001699.5:c.796G=	NP_001690.2:p.Asp266=
NM_001699.6:c.796G=	NP_001690.2:p.Asp266=
NM_021913.4:c.796G=	NP_068713.2:p.Asp266=
ENST00000301178.8:c.796G=	ENSP00000301178.3:p.Asp266=
ENST00000359092.7:c.796G=	ENSP00000351995.2:p.Asp266=
ENST00000593513.1:c.-9G=	ENSP00000471497.1:n.-9G=
ENST00000599659.5:n.810G=