Canonical Allele Identifier: CA346473137

Gene: ALK

Linked Data

• dbSNP Id: rs2148166628
• MyVariant Identifiers: chr2:g.29443672C>G (hg19) ; chr2:g.29220806C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220806C>G , CM000664.2:g.29220806C>G	GRCh38
NC_000002.11:g.29443672C>G , CM000664.1:g.29443672C>G	GRCh37
NC_000002.10:g.29297176C>G	NCBI36
NG_009445.1:g.705761G>C , LRG_488:g.705761G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3545G>C MANE Select	ENSP00000373700.3:p.Cys1182Ser
ENST00000431873.6:c.772G>C
ENST00000638605.1:n.422G>C
ENST00000642122.1:c.341G>C	ENSP00000493203.1:p.Cys114Ser
ENST00000389048.7:c.3545G>C	ENSP00000373700.3:p.Cys1182Ser
ENST00000431873.5:c.425G>C	ENSP00000414027.2:p.Cys142Ser
ENST00000618119.4:c.2414G>C	ENSP00000482733.1:p.Cys805Ser
NM_004304.4:c.3545G>C	NP_004295.2:p.Cys1182Ser
NM_001353765.1:c.341G>C	NP_001340694.1:p.Cys114Ser
XM_024452778.1:c.698G>C	XP_024308546.1:p.Cys233Ser
XM_024452779.1:c.341G>C	XP_024308547.1:p.Cys114Ser
NM_004304.5:c.3545G>C MANE Select	NP_004295.2:p.Cys1182Ser
NM_001353765.2:c.341G>C	NP_001340694.1:p.Cys114Ser