Canonical Allele Identifier: CA658655647

Gene: ALK

Linked Data

• ClinVar Variation Id: 470830
• ClinVar RCV Id: RCV000552569 ; RCV001020403
• dbSNP Id: rs1553394207

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222377_29222378delinsGT , CM000664.2:g.29222377_29222378delinsGT	GRCh38
NC_000002.11:g.29445243_29445244delinsGT , CM000664.1:g.29445243_29445244delinsGT	GRCh37
NC_000002.10:g.29298747_29298748delinsGT	NCBI36
NG_009445.1:g.704189_704190delinsAC , LRG_488:g.704189_704190delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3481_3482delinsAC MANE Select	ENSP00000373700.3:p.Glu1161Thr
ENST00000431873.6:c.708_709delinsAC
ENST00000638605.1:n.358_359delinsAC
ENST00000642122.1:c.277_278delinsAC	ENSP00000493203.1:p.Glu93Thr
ENST00000389048.7:c.3481_3482delinsAC	ENSP00000373700.3:p.Glu1161Thr
ENST00000431873.5:c.361_362delinsAC	ENSP00000414027.2:p.Glu121Thr
ENST00000453137.1:c.175_176delinsAC	ENSP00000387488.1:p.Glu59Thr
ENST00000618119.4:c.2350_2351delinsAC	ENSP00000482733.1:p.Glu784Thr
NM_004304.4:c.3481_3482delinsAC	NP_004295.2:p.Glu1161Thr
NM_001353765.1:c.277_278delinsAC	NP_001340694.1:p.Glu93Thr
XM_024452778.1:c.634_635delinsAC	XP_024308546.1:p.Glu212Thr
XM_024452779.1:c.277_278delinsAC	XP_024308547.1:p.Glu93Thr
NM_004304.5:c.3481_3482delinsAC MANE Select	NP_004295.2:p.Glu1161Thr
NM_001353765.2:c.277_278delinsAC	NP_001340694.1:p.Glu93Thr