Canonical Allele Identifier: CA425435208

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29223515C>T , CM000664.2:g.29223515C>T	GRCh38
NC_000002.11:g.29446381C>T , CM000664.1:g.29446381C>T	GRCh37
NC_000002.10:g.29299885C>T	NCBI36
NG_009445.1:g.703052G>A , LRG_488:g.703052G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004304.5:c.3186G>A MANE Select	NP_004295.2:p.Lys1062=
ENST00000389048.8:c.3186G>A MANE Select	ENSP00000373700.3:p.Lys1062=
NM_001353765.1:c.-19G>A	NP_001340694.1:n.-19G>A
NM_001353765.2:c.-19G>A	NP_001340694.1:n.-19G>A
NM_004304.4:c.3186G>A	NP_004295.2:p.Lys1062=
ENST00000389048.7:c.3186G>A	ENSP00000373700.3:p.Lys1062=
ENST00000431873.5:c.66G>A	ENSP00000414027.2:p.Lys22=
ENST00000431873.6:c.413G>A
ENST00000618119.4:c.2055G>A	ENSP00000482733.1:p.Lys685=
ENST00000638605.1:n.63G>A
ENST00000642122.1:c.-19G>A	ENSP00000493203.1:n.-19G>A
XM_024452778.1:c.339G>A	XP_024308546.1:p.Lys113=
XM_024452779.1:c.-19G>A	XP_024308547.1:n.-19G>A
XR_001738688.2:n.4042G>A