Canonical Allele Identifier: CA14661596

Gene: AXL

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41243143G>T , CM000681.2:g.41243143G>T	GRCh38
NC_000019.9:g.41749048G>T , CM000681.1:g.41749048G>T	GRCh37
NC_000019.8:g.46440888G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_021913.5:c.1445+128G>T MANE Select	NP_068713.2:n.1445+128G>T
ENST00000301178.9:c.1445+128G>T MANE Select	ENSP00000301178.3:n.1445+128G>T
NM_001278599.1:c.641+128G>T	NP_001265528.1:n.641+128G>T
NM_001278599.2:c.641+128G>T	NP_001265528.1:n.641+128G>T
NM_001699.5:c.1418+128G>T	NP_001690.2:n.1418+128G>T
NM_001699.6:c.1418+128G>T	NP_001690.2:n.1418+128G>T
NM_021913.4:c.1445+128G>T	NP_068713.2:n.1445+128G>T
ENST00000301178.8:c.1445+128G>T	ENSP00000301178.3:n.1445+128G>T
ENST00000359092.7:c.1418+128G>T	ENSP00000351995.2:n.1418+128G>T
ENST00000593513.1:c.641+128G>T	ENSP00000471497.1:n.641+128G>T
ENST00000599659.5:n.1459+128G>T