Canonical Allele Identifier: CA1241089797

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220804T= , CM000664.2:g.29220804T=	GRCh38
NC_000002.11:g.29443670T= , CM000664.1:g.29443670T=	GRCh37
NC_000002.10:g.29297174T=	NCBI36
NG_009445.1:g.705763A= , LRG_488:g.705763A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3547A= MANE Select	ENSP00000373700.3:p.Ile1183=
ENST00000431873.6:c.774A=
ENST00000638605.1:n.424A=
ENST00000642122.1:c.343A=	ENSP00000493203.1:p.Ile115=
ENST00000389048.7:c.3547A=	ENSP00000373700.3:p.Ile1183=
ENST00000431873.5:c.427A=	ENSP00000414027.2:p.Ile143=
ENST00000618119.4:c.2416A=	ENSP00000482733.1:p.Ile806=
NM_004304.4:c.3547A=	NP_004295.2:p.Ile1183=
NM_001353765.1:c.343A=	NP_001340694.1:p.Ile115=
XM_024452778.1:c.700A=	XP_024308546.1:p.Ile234=
XM_024452779.1:c.343A=	XP_024308547.1:p.Ile115=
NM_004304.5:c.3547A= MANE Select	NP_004295.2:p.Ile1183=
NM_001353765.2:c.343A=	NP_001340694.1:p.Ile115=