Canonical Allele Identifier: CA425619430

Gene: ALK

Linked Data

• dbSNP Id: rs878854655
• MyVariant Identifiers: chr2:g.29443665C>A (hg19)

Genomic Alleles

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

Transcript Alleles

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