Canonical Allele Identifier: CA1241089769

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220752G= , CM000664.2:g.29220752G=	GRCh38
NC_000002.11:g.29443618G= , CM000664.1:g.29443618G=	GRCh37
NC_000002.10:g.29297122G=	NCBI36
NG_009445.1:g.705815C= , LRG_488:g.705815C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3599C= MANE Select	ENSP00000373700.3:p.Ala1200=
ENST00000431873.6:c.826C=
ENST00000638605.1:n.476C=
ENST00000642122.1:c.395C=	ENSP00000493203.1:p.Ala132=
ENST00000389048.7:c.3599C=	ENSP00000373700.3:p.Ala1200=
ENST00000431873.5:c.479C=	ENSP00000414027.2:p.Ala160=
ENST00000618119.4:c.2468C=	ENSP00000482733.1:p.Ala823=
NM_004304.4:c.3599C=	NP_004295.2:p.Ala1200=
NM_001353765.1:c.395C=	NP_001340694.1:p.Ala132=
XM_024452778.1:c.752C=	XP_024308546.1:p.Ala251=
XM_024452779.1:c.395C=	XP_024308547.1:p.Ala132=
NM_004304.5:c.3599C= MANE Select	NP_004295.2:p.Ala1200=
NM_001353765.2:c.395C=	NP_001340694.1:p.Ala132=