Canonical Allele Identifier: CA346473153

Gene: ALK

Linked Data

• dbSNP Id: rs2148166668
• MyVariant Identifiers: chr2:g.29443681A>C (hg19) ; chr2:g.29220815A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220815A>C , CM000664.2:g.29220815A>C	GRCh38
NC_000002.11:g.29443681A>C , CM000664.1:g.29443681A>C	GRCh37
NC_000002.10:g.29297185A>C	NCBI36
NG_009445.1:g.705752T>G , LRG_488:g.705752T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3536T>G MANE Select	ENSP00000373700.3:p.Ile1179Ser
ENST00000431873.6:c.763T>G
ENST00000638605.1:n.413T>G
ENST00000642122.1:c.332T>G	ENSP00000493203.1:p.Ile111Ser
ENST00000389048.7:c.3536T>G	ENSP00000373700.3:p.Ile1179Ser
ENST00000431873.5:c.416T>G	ENSP00000414027.2:p.Ile139Ser
ENST00000618119.4:c.2405T>G	ENSP00000482733.1:p.Ile802Ser
NM_004304.4:c.3536T>G	NP_004295.2:p.Ile1179Ser
NM_001353765.1:c.332T>G	NP_001340694.1:p.Ile111Ser
XM_024452778.1:c.689T>G	XP_024308546.1:p.Ile230Ser
XM_024452779.1:c.332T>G	XP_024308547.1:p.Ile111Ser
NM_004304.5:c.3536T>G MANE Select	NP_004295.2:p.Ile1179Ser
NM_001353765.2:c.332T>G	NP_001340694.1:p.Ile111Ser