Canonical Allele Identifier: CA10581962

Gene: ALK

Linked Data

• ClinVar Variation Id: 239823
• ClinVar RCV Id: RCV000231498
• dbSNP Id: rs878854655
• gnomAD v4: 2-29220799-C-G
• MyVariant Identifiers: chr2:g.29443665C>G (hg19) ; chr2:g.29220799C>G (hg38)

Genomic Alleles

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

Transcript Alleles

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