Canonical Allele Identifier: CA2698809495

Gene: ALK

Linked Data

• dbSNP Id: rs1573120189

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220749_29220751del , CM000664.2:g.29220749_29220751del	GRCh38
NC_000002.11:g.29443615_29443617del , CM000664.1:g.29443615_29443617del	GRCh37
NC_000002.10:g.29297119_29297121del	NCBI36
NG_009445.1:g.705819_705821del , LRG_488:g.705819_705821del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3603_3605del MANE Select	ENSP00000373700.3:p.Gly1202del
ENST00000431873.6:c.830_832del
ENST00000638605.1:n.480_482del
ENST00000642122.1:c.399_401del	ENSP00000493203.1:p.Gly134del
ENST00000389048.7:c.3603_3605del	ENSP00000373700.3:p.Gly1202del
ENST00000431873.5:c.483_485del	ENSP00000414027.2:p.Gly162del
ENST00000618119.4:c.2472_2474del	ENSP00000482733.1:p.Gly825del
NM_004304.4:c.3603_3605del	NP_004295.2:p.Gly1202del
NM_001353765.1:c.399_401del	NP_001340694.1:p.Gly134del
XM_024452778.1:c.756_758del	XP_024308546.1:p.Gly253del
XM_024452779.1:c.399_401del	XP_024308547.1:p.Gly134del
NM_004304.5:c.3603_3605del MANE Select	NP_004295.2:p.Gly1202del
NM_001353765.2:c.399_401del	NP_001340694.1:p.Gly134del