Canonical Allele Identifier: CA346473161

Gene: ALK

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3533A>C MANE Select	ENSP00000373700.3:p.Asn1178Thr
ENST00000431873.6:c.760A>C
ENST00000638605.1:n.410A>C
ENST00000642122.1:c.329A>C	ENSP00000493203.1:p.Asn110Thr
ENST00000389048.7:c.3533A>C	ENSP00000373700.3:p.Asn1178Thr
ENST00000431873.5:c.413A>C	ENSP00000414027.2:p.Asn138Thr
ENST00000618119.4:c.2402A>C	ENSP00000482733.1:p.Asn801Thr
NM_004304.4:c.3533A>C	NP_004295.2:p.Asn1178Thr
NM_001353765.1:c.329A>C	NP_001340694.1:p.Asn110Thr
XM_024452778.1:c.686A>C	XP_024308546.1:p.Asn229Thr
XM_024452779.1:c.329A>C	XP_024308547.1:p.Asn110Thr
NM_004304.5:c.3533A>C MANE Select	NP_004295.2:p.Asn1178Thr
NM_001353765.2:c.329A>C	NP_001340694.1:p.Asn110Thr