Canonical Allele Identifier: CA1241090589

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222495T= , CM000664.2:g.29222495T=	GRCh38
NC_000002.11:g.29445361T= , CM000664.1:g.29445361T=	GRCh37
NC_000002.10:g.29298865T=	NCBI36
NG_009445.1:g.704072A= , LRG_488:g.704072A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.3450+22A= MANE Select	ENSP00000373700.3:n.3450+22A=
ENST00000431873.6:c.677+22A=
ENST00000638605.1:n.327+22A=
ENST00000642122.1:c.246+22A=	ENSP00000493203.1:n.246+22A=
ENST00000389048.7:c.3450+22A=	ENSP00000373700.3:n.3450+22A=
ENST00000431873.5:c.330+22A=	ENSP00000414027.2:n.330+22A=
ENST00000453137.1:c.144+22A=	ENSP00000387488.1:n.144+22A=
ENST00000618119.4:c.2319+22A=	ENSP00000482733.1:n.2319+22A=
NM_004304.4:c.3450+22A=	NP_004295.2:n.3450+22A=
NM_001353765.1:c.246+22A=	NP_001340694.1:n.246+22A=
XM_024452778.1:c.603+22A=	XP_024308546.1:n.603+22A=
XM_024452779.1:c.246+22A=	XP_024308547.1:n.246+22A=
NM_004304.5:c.3450+22A= MANE Select	NP_004295.2:n.3450+22A=
NM_001353765.2:c.246+22A=	NP_001340694.1:n.246+22A=