Canonical Allele Identifier: CA1241089770

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220754C= , CM000664.2:g.29220754C=	GRCh38
NC_000002.11:g.29443620C= , CM000664.1:g.29443620C=	GRCh37
NC_000002.10:g.29297124C=	NCBI36
NG_009445.1:g.705813G= , LRG_488:g.705813G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3597G= MANE Select	ENSP00000373700.3:p.Met1199=
ENST00000431873.6:c.824G=
ENST00000638605.1:n.474G=
ENST00000642122.1:c.393G=	ENSP00000493203.1:p.Met131=
ENST00000389048.7:c.3597G=	ENSP00000373700.3:p.Met1199=
ENST00000431873.5:c.477G=	ENSP00000414027.2:p.Met159=
ENST00000618119.4:c.2466G=	ENSP00000482733.1:p.Met822=
NM_004304.4:c.3597G=	NP_004295.2:p.Met1199=
NM_001353765.1:c.393G=	NP_001340694.1:p.Met131=
XM_024452778.1:c.750G=	XP_024308546.1:p.Met250=
XM_024452779.1:c.393G=	XP_024308547.1:p.Met131=
NM_004304.5:c.3597G= MANE Select	NP_004295.2:p.Met1199=
NM_001353765.2:c.393G=	NP_001340694.1:p.Met131=