Canonical Allele Identifier: CA9458098

Gene: AXL

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41238014C>T , CM000681.2:g.41238014C>T	GRCh38
NC_000019.9:g.41743919C>T , CM000681.1:g.41743919C>T	GRCh37
NC_000019.8:g.46435759C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_021913.5:c.854C>T MANE Select	NP_068713.2:p.Ser285Leu
ENST00000301178.9:c.854C>T MANE Select	ENSP00000301178.3:p.Ser285Leu
NM_001278599.1:c.50C>T	NP_001265528.1:p.Ser17Leu
NM_001278599.2:c.50C>T	NP_001265528.1:p.Ser17Leu
NM_001699.5:c.854C>T	NP_001690.2:p.Ser285Leu
NM_001699.6:c.854C>T	NP_001690.2:p.Ser285Leu
NM_021913.4:c.854C>T	NP_068713.2:p.Ser285Leu
ENST00000301178.8:c.854C>T	ENSP00000301178.3:p.Ser285Leu
ENST00000359092.7:c.854C>T	ENSP00000351995.2:p.Ser285Leu
ENST00000593513.1:c.50C>T	ENSP00000471497.1:p.Ser17Leu
ENST00000599659.5:n.868C>T