Canonical Allele Identifier: CA1241089792

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220796C= , CM000664.2:g.29220796C=	GRCh38
NC_000002.11:g.29443662C= , CM000664.1:g.29443662C=	GRCh37
NC_000002.10:g.29297166C=	NCBI36
NG_009445.1:g.705771G= , LRG_488:g.705771G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3555G= MANE Select	ENSP00000373700.3:p.Val1185=
ENST00000431873.6:c.782G=
ENST00000638605.1:n.432G=
ENST00000642122.1:c.351G=	ENSP00000493203.1:p.Val117=
ENST00000389048.7:c.3555G=	ENSP00000373700.3:p.Val1185=
ENST00000431873.5:c.435G=	ENSP00000414027.2:p.Val145=
ENST00000618119.4:c.2424G=	ENSP00000482733.1:p.Val808=
NM_004304.4:c.3555G=	NP_004295.2:p.Val1185=
NM_001353765.1:c.351G=	NP_001340694.1:p.Val117=
XM_024452778.1:c.708G=	XP_024308546.1:p.Val236=
XM_024452779.1:c.351G=	XP_024308547.1:p.Val117=
NM_004304.5:c.3555G= MANE Select	NP_004295.2:p.Val1185=
NM_001353765.2:c.351G=	NP_001340694.1:p.Val117=