Canonical Allele Identifier: CA346473131

Gene: ALK

Linked Data

• dbSNP Id: rs1002995598
• MyVariant Identifiers: chr2:g.29443669A>T (hg19) ; chr2:g.29220803A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220803A>T , CM000664.2:g.29220803A>T	GRCh38
NC_000002.11:g.29443669A>T , CM000664.1:g.29443669A>T	GRCh37
NC_000002.10:g.29297173A>T	NCBI36
NG_009445.1:g.705764T>A , LRG_488:g.705764T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3548T>A MANE Select	ENSP00000373700.3:p.Ile1183Asn
ENST00000431873.6:c.775T>A
ENST00000638605.1:n.425T>A
ENST00000642122.1:c.344T>A	ENSP00000493203.1:p.Ile115Asn
ENST00000389048.7:c.3548T>A	ENSP00000373700.3:p.Ile1183Asn
ENST00000431873.5:c.428T>A	ENSP00000414027.2:p.Ile143Asn
ENST00000618119.4:c.2417T>A	ENSP00000482733.1:p.Ile806Asn
NM_004304.4:c.3548T>A	NP_004295.2:p.Ile1183Asn
NM_001353765.1:c.344T>A	NP_001340694.1:p.Ile115Asn
XM_024452778.1:c.701T>A	XP_024308546.1:p.Ile234Asn
XM_024452779.1:c.344T>A	XP_024308547.1:p.Ile115Asn
NM_004304.5:c.3548T>A MANE Select	NP_004295.2:p.Ile1183Asn
NM_001353765.2:c.344T>A	NP_001340694.1:p.Ile115Asn