Canonical Allele Identifier: CA1241089804

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220827T= , CM000664.2:g.29220827T=	GRCh38
NC_000002.11:g.29443693T= , CM000664.1:g.29443693T=	GRCh37
NC_000002.10:g.29297197T=	NCBI36
NG_009445.1:g.705740A= , LRG_488:g.705740A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3524A= MANE Select	ENSP00000373700.3:p.Asn1175=
ENST00000431873.6:c.751A=
ENST00000638605.1:n.401A=
ENST00000642122.1:c.320A=	ENSP00000493203.1:p.Asn107=
ENST00000389048.7:c.3524A=	ENSP00000373700.3:p.Asn1175=
ENST00000431873.5:c.404A=	ENSP00000414027.2:p.Asn135=
ENST00000618119.4:c.2393A=	ENSP00000482733.1:p.Asn798=
NM_004304.4:c.3524A=	NP_004295.2:p.Asn1175=
NM_001353765.1:c.320A=	NP_001340694.1:p.Asn107=
XM_024452778.1:c.677A=	XP_024308546.1:p.Asn226=
XM_024452779.1:c.320A=	XP_024308547.1:p.Asn107=
NM_004304.5:c.3524A= MANE Select	NP_004295.2:p.Asn1175=
NM_001353765.2:c.320A=	NP_001340694.1:p.Asn107=