Canonical Allele Identifier: CA14689579

Gene: AXL

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41231439C>T , CM000681.2:g.41231439C>T	GRCh38
NC_000019.9:g.41737344C>T , CM000681.1:g.41737344C>T	GRCh37
NC_000019.8:g.46429184C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_021913.5:c.783+141C>T MANE Select	NP_068713.2:n.783+141C>T
ENST00000301178.9:c.783+141C>T MANE Select	ENSP00000301178.3:n.783+141C>T
NM_001278599.1:c.-22+141C>T	NP_001265528.1:n.-22+141C>T
NM_001278599.2:c.-22+141C>T	NP_001265528.1:n.-22+141C>T
NM_001699.5:c.783+141C>T	NP_001690.2:n.783+141C>T
NM_001699.6:c.783+141C>T	NP_001690.2:n.783+141C>T
NM_021913.4:c.783+141C>T	NP_068713.2:n.783+141C>T
ENST00000301178.8:c.783+141C>T	ENSP00000301178.3:n.783+141C>T
ENST00000359092.7:c.783+141C>T	ENSP00000351995.2:n.783+141C>T
ENST00000593513.1:c.-22+141C>T	ENSP00000471497.1:n.-22+141C>T
ENST00000599659.5:n.797+141C>T