Canonical Allele Identifier: CA346463211

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29445255G>T (hg19) ; chr2:g.29222389G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222389G>T , CM000664.2:g.29222389G>T	GRCh38
NC_000002.11:g.29445255G>T , CM000664.1:g.29445255G>T	GRCh37
NC_000002.10:g.29298759G>T	NCBI36
NG_009445.1:g.704178C>A , LRG_488:g.704178C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3470C>A MANE Select	ENSP00000373700.3:p.Ser1157Tyr
ENST00000431873.6:c.697C>A
ENST00000638605.1:n.347C>A
ENST00000642122.1:c.266C>A	ENSP00000493203.1:p.Ser89Tyr
ENST00000389048.7:c.3470C>A	ENSP00000373700.3:p.Ser1157Tyr
ENST00000431873.5:c.350C>A	ENSP00000414027.2:p.Ser117Tyr
ENST00000453137.1:c.164C>A	ENSP00000387488.1:p.Ser55Tyr
ENST00000618119.4:c.2339C>A	ENSP00000482733.1:p.Ser780Tyr
NM_004304.4:c.3470C>A	NP_004295.2:p.Ser1157Tyr
NM_001353765.1:c.266C>A	NP_001340694.1:p.Ser89Tyr
XM_024452778.1:c.623C>A	XP_024308546.1:p.Ser208Tyr
XM_024452779.1:c.266C>A	XP_024308547.1:p.Ser89Tyr
NM_004304.5:c.3470C>A MANE Select	NP_004295.2:p.Ser1157Tyr
NM_001353765.2:c.266C>A	NP_001340694.1:p.Ser89Tyr