Canonical Allele Identifier: CA346473160

Gene: ALK

Linked Data

• dbSNP Id: rs1669782434
• MyVariant Identifiers: chr2:g.29443683G>T (hg19) ; chr2:g.29220817G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220817G>T , CM000664.2:g.29220817G>T	GRCh38
NC_000002.11:g.29443683G>T , CM000664.1:g.29443683G>T	GRCh37
NC_000002.10:g.29297187G>T	NCBI36
NG_009445.1:g.705750C>A , LRG_488:g.705750C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3534C>A MANE Select	ENSP00000373700.3:p.Asn1178Lys
ENST00000431873.6:c.761C>A
ENST00000638605.1:n.411C>A
ENST00000642122.1:c.330C>A	ENSP00000493203.1:p.Asn110Lys
ENST00000389048.7:c.3534C>A	ENSP00000373700.3:p.Asn1178Lys
ENST00000431873.5:c.414C>A	ENSP00000414027.2:p.Asn138Lys
ENST00000618119.4:c.2403C>A	ENSP00000482733.1:p.Asn801Lys
NM_004304.4:c.3534C>A	NP_004295.2:p.Asn1178Lys
NM_001353765.1:c.330C>A	NP_001340694.1:p.Asn110Lys
XM_024452778.1:c.687C>A	XP_024308546.1:p.Asn229Lys
XM_024452779.1:c.330C>A	XP_024308547.1:p.Asn110Lys
NM_004304.5:c.3534C>A MANE Select	NP_004295.2:p.Asn1178Lys
NM_001353765.2:c.330C>A	NP_001340694.1:p.Asn110Lys