Canonical Allele Identifier: CA346473144

Gene: ALK

Linked Data

• dbSNP Id: rs56315533
• MyVariant Identifiers: chr2:g.29443676G>C (hg19) ; chr2:g.29220810G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220810G>C , CM000664.2:g.29220810G>C	GRCh38
NC_000002.11:g.29443676G>C , CM000664.1:g.29443676G>C	GRCh37
NC_000002.10:g.29297180G>C	NCBI36
NG_009445.1:g.705757C>G , LRG_488:g.705757C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3541C>G MANE Select	ENSP00000373700.3:p.Arg1181Gly
ENST00000431873.6:c.768C>G
ENST00000638605.1:n.418C>G
ENST00000642122.1:c.337C>G	ENSP00000493203.1:p.Arg113Gly
ENST00000389048.7:c.3541C>G	ENSP00000373700.3:p.Arg1181Gly
ENST00000431873.5:c.421C>G	ENSP00000414027.2:p.Arg141Gly
ENST00000618119.4:c.2410C>G	ENSP00000482733.1:p.Arg804Gly
NM_004304.4:c.3541C>G	NP_004295.2:p.Arg1181Gly
NM_001353765.1:c.337C>G	NP_001340694.1:p.Arg113Gly
XM_024452778.1:c.694C>G	XP_024308546.1:p.Arg232Gly
XM_024452779.1:c.337C>G	XP_024308547.1:p.Arg113Gly
NM_004304.5:c.3541C>G MANE Select	NP_004295.2:p.Arg1181Gly
NM_001353765.2:c.337C>G	NP_001340694.1:p.Arg113Gly