Canonical Allele Identifier: CA346473162

Gene: ALK

Linked Data

• dbSNP Id: rs2148166679
• MyVariant Identifiers: chr2:g.29443684T>C (hg19) ; chr2:g.29220818T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220818T>C , CM000664.2:g.29220818T>C	GRCh38
NC_000002.11:g.29443684T>C , CM000664.1:g.29443684T>C	GRCh37
NC_000002.10:g.29297188T>C	NCBI36
NG_009445.1:g.705749A>G , LRG_488:g.705749A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3533A>G MANE Select	ENSP00000373700.3:p.Asn1178Ser
ENST00000431873.6:c.760A>G
ENST00000638605.1:n.410A>G
ENST00000642122.1:c.329A>G	ENSP00000493203.1:p.Asn110Ser
ENST00000389048.7:c.3533A>G	ENSP00000373700.3:p.Asn1178Ser
ENST00000431873.5:c.413A>G	ENSP00000414027.2:p.Asn138Ser
ENST00000618119.4:c.2402A>G	ENSP00000482733.1:p.Asn801Ser
NM_004304.4:c.3533A>G	NP_004295.2:p.Asn1178Ser
NM_001353765.1:c.329A>G	NP_001340694.1:p.Asn110Ser
XM_024452778.1:c.686A>G	XP_024308546.1:p.Asn229Ser
XM_024452779.1:c.329A>G	XP_024308547.1:p.Asn110Ser
NM_004304.5:c.3533A>G MANE Select	NP_004295.2:p.Asn1178Ser
NM_001353765.2:c.329A>G	NP_001340694.1:p.Asn110Ser