Canonical Allele Identifier: CA995960686

Gene: AXL

Linked Data

• dbSNP Id: rs2034352541
• gnomAD v3: 19-41250962-G-A
• gnomAD v4: 19-41250962-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41250962G>A , CM000681.2:g.41250962G>A	GRCh38
NC_000019.9:g.41756867G>A , CM000681.1:g.41756867G>A	GRCh37
NC_000019.8:g.46448707G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000301178.9:c.1712-1389G>A MANE Select	ENSP00000301178.3:n.1712-1389G>A
ENST00000301178.8:c.1712-1389G>A	ENSP00000301178.3:n.1712-1389G>A
ENST00000359092.7:c.1685-1389G>A	ENSP00000351995.2:n.1685-1389G>A
ENST00000593513.1:c.908-1389G>A	ENSP00000471497.1:n.908-1389G>A
NM_001278599.1:c.908-1389G>A	NP_001265528.1:n.908-1389G>A
NM_001699.5:c.1685-1389G>A	NP_001690.2:n.1685-1389G>A
NM_021913.4:c.1712-1389G>A	NP_068713.2:n.1712-1389G>A
NM_021913.5:c.1712-1389G>A MANE Select	NP_068713.2:n.1712-1389G>A
NM_001699.6:c.1685-1389G>A	NP_001690.2:n.1685-1389G>A
NM_001278599.2:c.908-1389G>A	NP_001265528.1:n.908-1389G>A