Canonical Allele Identifier: CA346473104

Gene: ALK

Linked Data

• dbSNP Id: rs1669781283
• MyVariant Identifiers: chr2:g.29443655G>C (hg19) ; chr2:g.29220789G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220789G>C , CM000664.2:g.29220789G>C	GRCh38
NC_000002.11:g.29443655G>C , CM000664.1:g.29443655G>C	GRCh37
NC_000002.10:g.29297159G>C	NCBI36
NG_009445.1:g.705778C>G , LRG_488:g.705778C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3562C>G MANE Select	ENSP00000373700.3:p.Gln1188Glu
ENST00000431873.6:c.789C>G
ENST00000638605.1:n.439C>G
ENST00000642122.1:c.358C>G	ENSP00000493203.1:p.Gln120Glu
ENST00000389048.7:c.3562C>G	ENSP00000373700.3:p.Gln1188Glu
ENST00000431873.5:c.442C>G	ENSP00000414027.2:p.Gln148Glu
ENST00000618119.4:c.2431C>G	ENSP00000482733.1:p.Gln811Glu
NM_004304.4:c.3562C>G	NP_004295.2:p.Gln1188Glu
NM_001353765.1:c.358C>G	NP_001340694.1:p.Gln120Glu
XM_024452778.1:c.715C>G	XP_024308546.1:p.Gln239Glu
XM_024452779.1:c.358C>G	XP_024308547.1:p.Gln120Glu
NM_004304.5:c.3562C>G MANE Select	NP_004295.2:p.Gln1188Glu
NM_001353765.2:c.358C>G	NP_001340694.1:p.Gln120Glu