Canonical Allele Identifier: CA1241090487

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222315G= , CM000664.2:g.29222315G=	GRCh38
NC_000002.11:g.29445181G= , CM000664.1:g.29445181G=	GRCh37
NC_000002.10:g.29298685G=	NCBI36
NG_009445.1:g.704252C= , LRG_488:g.704252C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3515+29C= MANE Select	ENSP00000373700.3:n.3515+29C=
ENST00000431873.6:c.742+29C=
ENST00000638605.1:n.392+29C=
ENST00000642122.1:c.311+29C=	ENSP00000493203.1:n.311+29C=
ENST00000389048.7:c.3515+29C=	ENSP00000373700.3:n.3515+29C=
ENST00000431873.5:c.395+29C=	ENSP00000414027.2:n.395+29C=
ENST00000453137.1:c.209+29C=	ENSP00000387488.1:n.209+29C=
ENST00000618119.4:c.2384+29C=	ENSP00000482733.1:n.2384+29C=
NM_004304.4:c.3515+29C=	NP_004295.2:n.3515+29C=
NM_001353765.1:c.311+29C=	NP_001340694.1:n.311+29C=
XM_024452778.1:c.668+29C=	XP_024308546.1:n.668+29C=
XM_024452779.1:c.311+29C=	XP_024308547.1:n.311+29C=
NM_004304.5:c.3515+29C= MANE Select	NP_004295.2:n.3515+29C=
NM_001353765.2:c.311+29C=	NP_001340694.1:n.311+29C=