Canonical Allele Identifier: CA1241089790

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220789G= , CM000664.2:g.29220789G=	GRCh38
NC_000002.11:g.29443655G= , CM000664.1:g.29443655G=	GRCh37
NC_000002.10:g.29297159G=	NCBI36
NG_009445.1:g.705778C= , LRG_488:g.705778C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.3562C= MANE Select	ENSP00000373700.3:p.Gln1188=
ENST00000431873.6:c.789C=
ENST00000638605.1:n.439C=
ENST00000642122.1:c.358C=	ENSP00000493203.1:p.Gln120=
ENST00000389048.7:c.3562C=	ENSP00000373700.3:p.Gln1188=
ENST00000431873.5:c.442C=	ENSP00000414027.2:p.Gln148=
ENST00000618119.4:c.2431C=	ENSP00000482733.1:p.Gln811=
NM_004304.4:c.3562C=	NP_004295.2:p.Gln1188=
NM_001353765.1:c.358C=	NP_001340694.1:p.Gln120=
XM_024452778.1:c.715C=	XP_024308546.1:p.Gln239=
XM_024452779.1:c.358C=	XP_024308547.1:p.Gln120=
NM_004304.5:c.3562C= MANE Select	NP_004295.2:p.Gln1188=
NM_001353765.2:c.358C=	NP_001340694.1:p.Gln120=