Canonical Allele Identifier: CA1241089775

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220760C= , CM000664.2:g.29220760C=	GRCh38
NC_000002.11:g.29443626C= , CM000664.1:g.29443626C=	GRCh37
NC_000002.10:g.29297130C=	NCBI36
NG_009445.1:g.705807G= , LRG_488:g.705807G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3591G= MANE Select	ENSP00000373700.3:p.Glu1197=
ENST00000431873.6:c.818G=
ENST00000638605.1:n.468G=
ENST00000642122.1:c.387G=	ENSP00000493203.1:p.Glu129=
ENST00000389048.7:c.3591G=	ENSP00000373700.3:p.Glu1197=
ENST00000431873.5:c.471G=	ENSP00000414027.2:p.Glu157=
ENST00000618119.4:c.2460G=	ENSP00000482733.1:p.Glu820=
NM_004304.4:c.3591G=	NP_004295.2:p.Glu1197=
NM_001353765.1:c.387G=	NP_001340694.1:p.Glu129=
XM_024452778.1:c.744G=	XP_024308546.1:p.Glu248=
XM_024452779.1:c.387G=	XP_024308547.1:p.Glu129=
NM_004304.5:c.3591G= MANE Select	NP_004295.2:p.Glu1197=
NM_001353765.2:c.387G=	NP_001340694.1:p.Glu129=