Canonical Allele Identifier: CA882329845

Gene: AXL

Linked Data

• dbSNP Id: rs1216250511
• gnomAD v3: 19-41250760-GAC-G
• gnomAD v4: 19-41250760-GAC-G
• MyVariant Identifiers: chr19:g.41756666_41756667del (hg19) ; chr19:g.41250761_41250762del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41250762_41250763del , CM000681.2:g.41250762_41250763del	GRCh38
NC_000019.9:g.41756667_41756668del , CM000681.1:g.41756667_41756668del	GRCh37
NC_000019.8:g.46448507_46448508del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301178.9:c.1712-1589_1712-1588del MANE Select	ENSP00000301178.3:n.1712-1589_1712-1588del
ENST00000301178.8:c.1712-1589_1712-1588del	ENSP00000301178.3:n.1712-1589_1712-1588del
ENST00000359092.7:c.1685-1589_1685-1588del	ENSP00000351995.2:n.1685-1589_1685-1588del
ENST00000593513.1:c.908-1589_908-1588del	ENSP00000471497.1:n.908-1589_908-1588del
NM_001278599.1:c.908-1589_908-1588del	NP_001265528.1:n.908-1589_908-1588del
NM_001699.5:c.1685-1589_1685-1588del	NP_001690.2:n.1685-1589_1685-1588del
NM_021913.4:c.1712-1589_1712-1588del	NP_068713.2:n.1712-1589_1712-1588del
NM_021913.5:c.1712-1589_1712-1588del MANE Select	NP_068713.2:n.1712-1589_1712-1588del
NM_001699.6:c.1685-1589_1685-1588del	NP_001690.2:n.1685-1589_1685-1588del
NM_001278599.2:c.908-1589_908-1588del	NP_001265528.1:n.908-1589_908-1588del