Canonical Allele Identifier: CA1241089763

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220746C= , CM000664.2:g.29220746C=	GRCh38
NC_000002.11:g.29443612C= , CM000664.1:g.29443612C=	GRCh37
NC_000002.10:g.29297116C=	NCBI36
NG_009445.1:g.705821G= , LRG_488:g.705821G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3605G= MANE Select	ENSP00000373700.3:p.Gly1202=
ENST00000431873.6:c.832G=
ENST00000638605.1:n.482G=
ENST00000642122.1:c.401G=	ENSP00000493203.1:p.Gly134=
ENST00000389048.7:c.3605G=	ENSP00000373700.3:p.Gly1202=
ENST00000431873.5:c.485G=	ENSP00000414027.2:p.Gly162=
ENST00000618119.4:c.2474G=	ENSP00000482733.1:p.Gly825=
NM_004304.4:c.3605G=	NP_004295.2:p.Gly1202=
NM_001353765.1:c.401G=	NP_001340694.1:p.Gly134=
XM_024452778.1:c.758G=	XP_024308546.1:p.Gly253=
XM_024452779.1:c.401G=	XP_024308547.1:p.Gly134=
NM_004304.5:c.3605G= MANE Select	NP_004295.2:p.Gly1202=
NM_001353765.2:c.401G=	NP_001340694.1:p.Gly134=