Canonical Allele Identifier: CA425619431

Gene: ALK

Linked Data

• ClinVar Variation Id: 2875543
• ClinVar RCV Id: RCV003633221
• dbSNP Id: rs878854655
• MyVariant Identifiers: chr2:g.29443665C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220799C>T , CM000664.2:g.29220799C>T	GRCh38
NC_000002.11:g.29443665C>T , CM000664.1:g.29443665C>T	GRCh37
NC_000002.10:g.29297169C>T	NCBI36
NG_009445.1:g.705768G>A , LRG_488:g.705768G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3552G>A MANE Select	ENSP00000373700.3:p.Gly1184=
ENST00000431873.6:c.779G>A
ENST00000638605.1:n.429G>A
ENST00000642122.1:c.348G>A	ENSP00000493203.1:p.Gly116=
ENST00000389048.7:c.3552G>A	ENSP00000373700.3:p.Gly1184=
ENST00000431873.5:c.432G>A	ENSP00000414027.2:p.Gly144=
ENST00000618119.4:c.2421G>A	ENSP00000482733.1:p.Gly807=
NM_004304.4:c.3552G>A	NP_004295.2:p.Gly1184=
NM_001353765.1:c.348G>A	NP_001340694.1:p.Gly116=
XM_024452778.1:c.705G>A	XP_024308546.1:p.Gly235=
XM_024452779.1:c.348G>A	XP_024308547.1:p.Gly116=
NM_004304.5:c.3552G>A MANE Select	NP_004295.2:p.Gly1184=
NM_001353765.2:c.348G>A	NP_001340694.1:p.Gly116=