Canonical Allele Identifier: CA2735946355

Gene: AXL

Linked Data

• dbSNP Id: rs2122270391

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41250765_41250766del , CM000681.2:g.41250765_41250766del	GRCh38
NC_000019.9:g.41756670_41756671del , CM000681.1:g.41756670_41756671del	GRCh37
NC_000019.8:g.46448510_46448511del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301178.9:c.1712-1586_1712-1585del MANE Select	ENSP00000301178.3:n.1712-1586_1712-1585del
ENST00000301178.8:c.1712-1586_1712-1585del	ENSP00000301178.3:n.1712-1586_1712-1585del
ENST00000359092.7:c.1685-1586_1685-1585del	ENSP00000351995.2:n.1685-1586_1685-1585del
ENST00000593513.1:c.908-1586_908-1585del	ENSP00000471497.1:n.908-1586_908-1585del
NM_001278599.1:c.908-1586_908-1585del	NP_001265528.1:n.908-1586_908-1585del
NM_001699.5:c.1685-1586_1685-1585del	NP_001690.2:n.1685-1586_1685-1585del
NM_021913.4:c.1712-1586_1712-1585del	NP_068713.2:n.1712-1586_1712-1585del
NM_021913.5:c.1712-1586_1712-1585del MANE Select	NP_068713.2:n.1712-1586_1712-1585del
NM_001699.6:c.1685-1586_1685-1585del	NP_001690.2:n.1685-1586_1685-1585del
NM_001278599.2:c.908-1586_908-1585del	NP_001265528.1:n.908-1586_908-1585del