Canonical Allele Identifier: CA1241083968

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29209873A= , CM000664.2:g.29209873A=	GRCh38
NC_000002.11:g.29432739A= , CM000664.1:g.29432739A=	GRCh37
NC_000002.10:g.29286243A=	NCBI36
NG_009445.1:g.716694T= , LRG_488:g.716694T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3749T= MANE Select	ENSP00000373700.3:p.Ile1250=
ENST00000431873.6:c.976T=
ENST00000638605.1:n.626T=
ENST00000642122.1:c.545T=	ENSP00000493203.1:p.Ile182=
ENST00000389048.7:c.3749T=	ENSP00000373700.3:p.Ile1250=
ENST00000431873.5:c.629T=	ENSP00000414027.2:p.Ile210=
ENST00000618119.4:c.2618T=	ENSP00000482733.1:p.Ile873=
NM_004304.4:c.3749T=	NP_004295.2:p.Ile1250=
NM_001353765.1:c.545T=	NP_001340694.1:p.Ile182=
XM_024452778.1:c.902T=	XP_024308546.1:p.Ile301=
XM_024452779.1:c.545T=	XP_024308547.1:p.Ile182=
NM_004304.5:c.3749T= MANE Select	NP_004295.2:p.Ile1250=
NM_001353765.2:c.545T=	NP_001340694.1:p.Ile182=