Canonical Allele Identifier: CA1241089759

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220740A= , CM000664.2:g.29220740A=	GRCh38
NC_000002.11:g.29443606A= , CM000664.1:g.29443606A=	GRCh37
NC_000002.10:g.29297110A=	NCBI36
NG_009445.1:g.705827T= , LRG_488:g.705827T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3611T= MANE Select	ENSP00000373700.3:p.Leu1204=
ENST00000431873.6:c.838T=
ENST00000638605.1:n.488T=
ENST00000642122.1:c.407T=	ENSP00000493203.1:p.Leu136=
ENST00000389048.7:c.3611T=	ENSP00000373700.3:p.Leu1204=
ENST00000431873.5:c.491T=	ENSP00000414027.2:p.Leu164=
ENST00000618119.4:c.2480T=	ENSP00000482733.1:p.Leu827=
NM_004304.4:c.3611T=	NP_004295.2:p.Leu1204=
NM_001353765.1:c.407T=	NP_001340694.1:p.Leu136=
XM_024452778.1:c.764T=	XP_024308546.1:p.Leu255=
XM_024452779.1:c.407T=	XP_024308547.1:p.Leu136=
NM_004304.5:c.3611T= MANE Select	NP_004295.2:p.Leu1204=
NM_001353765.2:c.407T=	NP_001340694.1:p.Leu136=