Canonical Allele Identifier: CA2336378178

Gene: AXL

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41250917G= , CM000681.2:g.41250917G=	GRCh38
NC_000019.9:g.41756822G= , CM000681.1:g.41756822G=	GRCh37
NC_000019.8:g.46448662G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000301178.9:c.1712-1434G= MANE Select	ENSP00000301178.3:n.1712-1434G=
ENST00000301178.8:c.1712-1434G=	ENSP00000301178.3:n.1712-1434G=
ENST00000359092.7:c.1685-1434G=	ENSP00000351995.2:n.1685-1434G=
ENST00000593513.1:c.908-1434G=	ENSP00000471497.1:n.908-1434G=
NM_001278599.1:c.908-1434G=	NP_001265528.1:n.908-1434G=
NM_001699.5:c.1685-1434G=	NP_001690.2:n.1685-1434G=
NM_021913.4:c.1712-1434G=	NP_068713.2:n.1712-1434G=
NM_021913.5:c.1712-1434G= MANE Select	NP_068713.2:n.1712-1434G=
NM_001699.6:c.1685-1434G=	NP_001690.2:n.1685-1434G=
NM_001278599.2:c.908-1434G=	NP_001265528.1:n.908-1434G=