Canonical Allele Identifier: CA1241089743

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220704A= , CM000664.2:g.29220704A=	GRCh38
NC_000002.11:g.29443570A= , CM000664.1:g.29443570A=	GRCh37
NC_000002.10:g.29297074A=	NCBI36
NG_009445.1:g.705863T= , LRG_488:g.705863T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3645+2T= MANE Select	ENSP00000373700.3:n.3645+2T=
ENST00000431873.6:c.872+2T=
ENST00000638605.1:n.522+2T=
ENST00000642122.1:c.441+2T=	ENSP00000493203.1:n.441+2T=
ENST00000389048.7:c.3645+2T=	ENSP00000373700.3:n.3645+2T=
ENST00000431873.5:c.525+2T=	ENSP00000414027.2:n.525+2T=
ENST00000618119.4:c.2514+2T=	ENSP00000482733.1:n.2514+2T=
NM_004304.4:c.3645+2T=	NP_004295.2:n.3645+2T=
NM_001353765.1:c.441+2T=	NP_001340694.1:n.441+2T=
XM_024452778.1:c.798+2T=	XP_024308546.1:n.798+2T=
XM_024452779.1:c.441+2T=	XP_024308547.1:n.441+2T=
NM_004304.5:c.3645+2T= MANE Select	NP_004295.2:n.3645+2T=
NM_001353765.2:c.441+2T=	NP_001340694.1:n.441+2T=