Canonical Allele Identifier: CA1241090538

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222407G= , CM000664.2:g.29222407G=	GRCh38
NC_000002.11:g.29445273G= , CM000664.1:g.29445273G=	GRCh37
NC_000002.10:g.29298777G=	NCBI36
NG_009445.1:g.704160C= , LRG_488:g.704160C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3452C= MANE Select	ENSP00000373700.3:p.Thr1151=
ENST00000431873.6:c.679C=
ENST00000638605.1:n.329C=
ENST00000642122.1:c.248C=	ENSP00000493203.1:p.Thr83=
ENST00000389048.7:c.3452C=	ENSP00000373700.3:p.Thr1151=
ENST00000431873.5:c.332C=	ENSP00000414027.2:p.Thr111=
ENST00000453137.1:c.146C=	ENSP00000387488.1:p.Thr49=
ENST00000618119.4:c.2321C=	ENSP00000482733.1:p.Thr774=
NM_004304.4:c.3452C=	NP_004295.2:p.Thr1151=
NM_001353765.1:c.248C=	NP_001340694.1:p.Thr83=
XM_024452778.1:c.605C=	XP_024308546.1:p.Thr202=
XM_024452779.1:c.248C=	XP_024308547.1:p.Thr83=
NM_004304.5:c.3452C= MANE Select	NP_004295.2:p.Thr1151=
NM_001353765.2:c.248C=	NP_001340694.1:p.Thr83=