Canonical Allele Identifier: CA346463194

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29445252T>G (hg19) ; chr2:g.29222386T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222386T>G , CM000664.2:g.29222386T>G	GRCh38
NC_000002.11:g.29445252T>G , CM000664.1:g.29445252T>G	GRCh37
NC_000002.10:g.29298756T>G	NCBI36
NG_009445.1:g.704181A>C , LRG_488:g.704181A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3473A>C MANE Select	ENSP00000373700.3:p.Glu1158Ala
ENST00000431873.6:c.700A>C
ENST00000638605.1:n.350A>C
ENST00000642122.1:c.269A>C	ENSP00000493203.1:p.Glu90Ala
ENST00000389048.7:c.3473A>C	ENSP00000373700.3:p.Glu1158Ala
ENST00000431873.5:c.353A>C	ENSP00000414027.2:p.Glu118Ala
ENST00000453137.1:c.167A>C	ENSP00000387488.1:p.Glu56Ala
ENST00000618119.4:c.2342A>C	ENSP00000482733.1:p.Glu781Ala
NM_004304.4:c.3473A>C	NP_004295.2:p.Glu1158Ala
NM_001353765.1:c.269A>C	NP_001340694.1:p.Glu90Ala
XM_024452778.1:c.626A>C	XP_024308546.1:p.Glu209Ala
XM_024452779.1:c.269A>C	XP_024308547.1:p.Glu90Ala
NM_004304.5:c.3473A>C MANE Select	NP_004295.2:p.Glu1158Ala
NM_001353765.2:c.269A>C	NP_001340694.1:p.Glu90Ala