Canonical Allele Identifier: CA308548877

Gene: AXL

Linked Data

• dbSNP Id: rs994831482
• gnomAD v2: 19-41756909-G-T
• gnomAD v3: 19-41251004-G-T
• gnomAD v4: 19-41251004-G-T
• MyVariant Identifiers: chr19:g.41756909G>T (hg19) ; chr19:g.41251004G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41251004G>T , CM000681.2:g.41251004G>T	GRCh38
NC_000019.9:g.41756909G>T , CM000681.1:g.41756909G>T	GRCh37
NC_000019.8:g.46448749G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301178.9:c.1712-1347G>T MANE Select	ENSP00000301178.3:n.1712-1347G>T
ENST00000301178.8:c.1712-1347G>T	ENSP00000301178.3:n.1712-1347G>T
ENST00000359092.7:c.1685-1347G>T	ENSP00000351995.2:n.1685-1347G>T
ENST00000593513.1:c.908-1347G>T	ENSP00000471497.1:n.908-1347G>T
NM_001278599.1:c.908-1347G>T	NP_001265528.1:n.908-1347G>T
NM_001699.5:c.1685-1347G>T	NP_001690.2:n.1685-1347G>T
NM_021913.4:c.1712-1347G>T	NP_068713.2:n.1712-1347G>T
NM_021913.5:c.1712-1347G>T MANE Select	NP_068713.2:n.1712-1347G>T
NM_001699.6:c.1685-1347G>T	NP_001690.2:n.1685-1347G>T
NM_001278599.2:c.908-1347G>T	NP_001265528.1:n.908-1347G>T