Canonical Allele Identifier: CA1241089771

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220756T= , CM000664.2:g.29220756T=	GRCh38
NC_000002.11:g.29443622T= , CM000664.1:g.29443622T=	GRCh37
NC_000002.10:g.29297126T=	NCBI36
NG_009445.1:g.705811A= , LRG_488:g.705811A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3595A= MANE Select	ENSP00000373700.3:p.Met1199=
ENST00000431873.6:c.822A=
ENST00000638605.1:n.472A=
ENST00000642122.1:c.391A=	ENSP00000493203.1:p.Met131=
ENST00000389048.7:c.3595A=	ENSP00000373700.3:p.Met1199=
ENST00000431873.5:c.475A=	ENSP00000414027.2:p.Met159=
ENST00000618119.4:c.2464A=	ENSP00000482733.1:p.Met822=
NM_004304.4:c.3595A=	NP_004295.2:p.Met1199=
NM_001353765.1:c.391A=	NP_001340694.1:p.Met131=
XM_024452778.1:c.748A=	XP_024308546.1:p.Met250=
XM_024452779.1:c.391A=	XP_024308547.1:p.Met131=
NM_004304.5:c.3595A= MANE Select	NP_004295.2:p.Met1199=
NM_001353765.2:c.391A=	NP_001340694.1:p.Met131=