Canonical Allele Identifier: CA1241089788

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220785G= , CM000664.2:g.29220785G=	GRCh38
NC_000002.11:g.29443651G= , CM000664.1:g.29443651G=	GRCh37
NC_000002.10:g.29297155G=	NCBI36
NG_009445.1:g.705782C= , LRG_488:g.705782C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.3566C= MANE Select	ENSP00000373700.3:p.Ser1189=
ENST00000431873.6:c.793C=
ENST00000638605.1:n.443C=
ENST00000642122.1:c.362C=	ENSP00000493203.1:p.Ser121=
ENST00000389048.7:c.3566C=	ENSP00000373700.3:p.Ser1189=
ENST00000431873.5:c.446C=	ENSP00000414027.2:p.Ser149=
ENST00000618119.4:c.2435C=	ENSP00000482733.1:p.Ser812=
NM_004304.4:c.3566C=	NP_004295.2:p.Ser1189=
NM_001353765.1:c.362C=	NP_001340694.1:p.Ser121=
XM_024452778.1:c.719C=	XP_024308546.1:p.Ser240=
XM_024452779.1:c.362C=	XP_024308547.1:p.Ser121=
NM_004304.5:c.3566C= MANE Select	NP_004295.2:p.Ser1189=
NM_001353765.2:c.362C=	NP_001340694.1:p.Ser121=