Canonical Allele Identifier: CA1241089800

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220816T= , CM000664.2:g.29220816T=	GRCh38
NC_000002.11:g.29443682T= , CM000664.1:g.29443682T=	GRCh37
NC_000002.10:g.29297186T=	NCBI36
NG_009445.1:g.705751A= , LRG_488:g.705751A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3535A= MANE Select	ENSP00000373700.3:p.Ile1179=
ENST00000431873.6:c.762A=
ENST00000638605.1:n.412A=
ENST00000642122.1:c.331A=	ENSP00000493203.1:p.Ile111=
ENST00000389048.7:c.3535A=	ENSP00000373700.3:p.Ile1179=
ENST00000431873.5:c.415A=	ENSP00000414027.2:p.Ile139=
ENST00000618119.4:c.2404A=	ENSP00000482733.1:p.Ile802=
NM_004304.4:c.3535A=	NP_004295.2:p.Ile1179=
NM_001353765.1:c.331A=	NP_001340694.1:p.Ile111=
XM_024452778.1:c.688A=	XP_024308546.1:p.Ile230=
XM_024452779.1:c.331A=	XP_024308547.1:p.Ile111=
NM_004304.5:c.3535A= MANE Select	NP_004295.2:p.Ile1179=
NM_001353765.2:c.331A=	NP_001340694.1:p.Ile111=