Canonical Allele Identifier: CA1241083930

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29209798C= , CM000664.2:g.29209798C=	GRCh38
NC_000002.11:g.29432664C= , CM000664.1:g.29432664C=	GRCh37
NC_000002.10:g.29286168C=	NCBI36
NG_009445.1:g.716769G= , LRG_488:g.716769G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004304.5:c.3824G= MANE Select	NP_004295.2:p.Arg1275=
ENST00000389048.8:c.3824G= MANE Select	ENSP00000373700.3:p.Arg1275=
NM_001353765.1:c.620G=	NP_001340694.1:p.Arg207=
NM_001353765.2:c.620G=	NP_001340694.1:p.Arg207=
NM_004304.4:c.3824G=	NP_004295.2:p.Arg1275=
ENST00000389048.7:c.3824G=	ENSP00000373700.3:p.Arg1275=
ENST00000431873.5:c.704G=	ENSP00000414027.2:p.Arg235=
ENST00000431873.6:c.1051G=
ENST00000618119.4:c.2693G=	ENSP00000482733.1:p.Arg898=
ENST00000638605.1:n.701G=
ENST00000642122.1:c.620G=	ENSP00000493203.1:p.Arg207=
XM_024452778.1:c.977G=	XP_024308546.1:p.Arg326=
XM_024452779.1:c.620G=	XP_024308547.1:p.Arg207=