Canonical Allele Identifier: CA1241090644

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222584C= , CM000664.2:g.29222584C=	GRCh38
NC_000002.11:g.29445450C= , CM000664.1:g.29445450C=	GRCh37
NC_000002.10:g.29298954C=	NCBI36
NG_009445.1:g.703983G= , LRG_488:g.703983G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004304.5:c.3383G= MANE Select	NP_004295.2:p.Gly1128=
ENST00000389048.8:c.3383G= MANE Select	ENSP00000373700.3:p.Gly1128=
NM_001353765.1:c.179G=	NP_001340694.1:p.Gly60=
NM_001353765.2:c.179G=	NP_001340694.1:p.Gly60=
NM_004304.4:c.3383G=	NP_004295.2:p.Gly1128=
ENST00000389048.7:c.3383G=	ENSP00000373700.3:p.Gly1128=
ENST00000431873.5:c.263G=	ENSP00000414027.2:p.Gly88=
ENST00000431873.6:c.610G=
ENST00000453137.1:c.77G=	ENSP00000387488.1:p.Gly26=
ENST00000618119.4:c.2252G=	ENSP00000482733.1:p.Gly751=
ENST00000638605.1:n.260G=
ENST00000642122.1:c.179G=	ENSP00000493203.1:p.Gly60=
XM_024452778.1:c.536G=	XP_024308546.1:p.Gly179=
XM_024452779.1:c.179G=	XP_024308547.1:p.Gly60=