Canonical Allele Identifier: CA1241090452

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222243A= , CM000664.2:g.29222243A=	GRCh38
NC_000002.11:g.29445109A= , CM000664.1:g.29445109A=	GRCh37
NC_000002.10:g.29298613A=	NCBI36
NG_009445.1:g.704324T= , LRG_488:g.704324T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3515+101T= MANE Select	ENSP00000373700.3:n.3515+101T=
ENST00000431873.6:c.742+101T=
ENST00000638605.1:n.392+101T=
ENST00000642122.1:c.311+101T=	ENSP00000493203.1:n.311+101T=
ENST00000389048.7:c.3515+101T=	ENSP00000373700.3:n.3515+101T=
ENST00000431873.5:c.395+101T=	ENSP00000414027.2:n.395+101T=
ENST00000453137.1:c.209+101T=	ENSP00000387488.1:n.209+101T=
ENST00000618119.4:c.2384+101T=	ENSP00000482733.1:n.2384+101T=
NM_004304.4:c.3515+101T=	NP_004295.2:n.3515+101T=
NM_001353765.1:c.311+101T=	NP_001340694.1:n.311+101T=
XM_024452778.1:c.668+101T=	XP_024308546.1:n.668+101T=
XM_024452779.1:c.311+101T=	XP_024308547.1:n.311+101T=
NM_004304.5:c.3515+101T= MANE Select	NP_004295.2:n.3515+101T=
NM_001353765.2:c.311+101T=	NP_001340694.1:n.311+101T=