Canonical Allele Identifier: CA645528801

Gene: ALK

Linked Data

• COSMIC: COSM236271

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222361_29222362delinsAT , CM000664.2:g.29222361_29222362delinsAT	GRCh38
NC_000002.11:g.29445227_29445228delinsAT , CM000664.1:g.29445227_29445228delinsAT	GRCh37
NC_000002.10:g.29298731_29298732delinsAT	NCBI36
NG_009445.1:g.704205_704206delinsAT , LRG_488:g.704205_704206delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3497_3498delinsAT MANE Select	ENSP00000373700.3:p.Met1166Asn
ENST00000431873.6:c.724_725delinsAT
ENST00000638605.1:n.374_375delinsAT
ENST00000642122.1:c.293_294delinsAT	ENSP00000493203.1:p.Met98Asn
ENST00000389048.7:c.3497_3498delinsAT	ENSP00000373700.3:p.Met1166Asn
ENST00000431873.5:c.377_378delinsAT	ENSP00000414027.2:p.Met126Asn
ENST00000453137.1:c.191_192delinsAT	ENSP00000387488.1:p.Met64Asn
ENST00000618119.4:c.2366_2367delinsAT	ENSP00000482733.1:p.Met789Asn
NM_004304.4:c.3497_3498delinsAT	NP_004295.2:p.Met1166Asn
NM_001353765.1:c.293_294delinsAT	NP_001340694.1:p.Met98Asn
XM_024452778.1:c.650_651delinsAT	XP_024308546.1:p.Met217Asn
XM_024452779.1:c.293_294delinsAT	XP_024308547.1:p.Met98Asn
NM_004304.5:c.3497_3498delinsAT MANE Select	NP_004295.2:p.Met1166Asn
NM_001353765.2:c.293_294delinsAT	NP_001340694.1:p.Met98Asn