Canonical Allele Identifier: CA1241091059

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29223441G= , CM000664.2:g.29223441G=	GRCh38
NC_000002.11:g.29446307G= , CM000664.1:g.29446307G=	GRCh37
NC_000002.10:g.29299811G=	NCBI36
NG_009445.1:g.703126C= , LRG_488:g.703126C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3260C= MANE Select	ENSP00000373700.3:p.Thr1087=
ENST00000431873.6:c.487C=
ENST00000638605.1:n.137C=
ENST00000642122.1:c.56C=	ENSP00000493203.1:p.Thr19=
ENST00000389048.7:c.3260C=	ENSP00000373700.3:p.Thr1087=
ENST00000431873.5:c.140C=	ENSP00000414027.2:p.Thr47=
ENST00000618119.4:c.2129C=	ENSP00000482733.1:p.Thr710=
NM_004304.4:c.3260C=	NP_004295.2:p.Thr1087=
NM_001353765.1:c.56C=	NP_001340694.1:p.Thr19=
XM_024452778.1:c.413C=	XP_024308546.1:p.Thr138=
XM_024452779.1:c.56C=	XP_024308547.1:p.Thr19=
NM_004304.5:c.3260C= MANE Select	NP_004295.2:p.Thr1087=
NM_001353765.2:c.56C=	NP_001340694.1:p.Thr19=