Canonical Allele Identifier: CA1241090511

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222350A= , CM000664.2:g.29222350A=	GRCh38
NC_000002.11:g.29445216A= , CM000664.1:g.29445216A=	GRCh37
NC_000002.10:g.29298720A=	NCBI36
NG_009445.1:g.704217T= , LRG_488:g.704217T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3509T= MANE Select	ENSP00000373700.3:p.Ile1170=
ENST00000431873.6:c.736T=
ENST00000638605.1:n.386T=
ENST00000642122.1:c.305T=	ENSP00000493203.1:p.Ile102=
ENST00000389048.7:c.3509T=	ENSP00000373700.3:p.Ile1170=
ENST00000431873.5:c.389T=	ENSP00000414027.2:p.Ile130=
ENST00000453137.1:c.203T=	ENSP00000387488.1:p.Ile68=
ENST00000618119.4:c.2378T=	ENSP00000482733.1:p.Ile793=
NM_004304.4:c.3509T=	NP_004295.2:p.Ile1170=
NM_001353765.1:c.305T=	NP_001340694.1:p.Ile102=
XM_024452778.1:c.662T=	XP_024308546.1:p.Ile221=
XM_024452779.1:c.305T=	XP_024308547.1:p.Ile102=
NM_004304.5:c.3509T= MANE Select	NP_004295.2:p.Ile1170=
NM_001353765.2:c.305T=	NP_001340694.1:p.Ile102=