Canonical Allele Identifier: CA1241090498

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222326_29222328delinsGTC , CM000664.2:g.29222326_29222328delinsGTC	GRCh38
NC_000002.11:g.29445192_29445194delinsGTC , CM000664.1:g.29445192_29445194delinsGTC	GRCh37
NC_000002.10:g.29298696_29298698delinsGTC	NCBI36
NG_009445.1:g.704239_704241delinsGAC , LRG_488:g.704239_704241delinsGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3515+16_3515+18delinsGAC MANE Select	ENSP00000373700.3:n.3515+16_3515+18delinsGAC
ENST00000431873.6:c.742+16_742+18delinsGAC
ENST00000638605.1:n.392+16_392+18delinsGAC
ENST00000642122.1:c.311+16_311+18delinsGAC	ENSP00000493203.1:n.311+16_311+18delinsGAC
ENST00000389048.7:c.3515+16_3515+18delinsGAC	ENSP00000373700.3:n.3515+16_3515+18delinsGAC
ENST00000431873.5:c.395+16_395+18delinsGAC	ENSP00000414027.2:n.395+16_395+18delinsGAC
ENST00000453137.1:c.209+16_209+18delinsGAC	ENSP00000387488.1:n.209+16_209+18delinsGAC
ENST00000618119.4:c.2384+16_2384+18delinsGAC	ENSP00000482733.1:n.2384+16_2384+18delinsGAC
NM_004304.4:c.3515+16_3515+18delinsGAC	NP_004295.2:n.3515+16_3515+18delinsGAC
NM_001353765.1:c.311+16_311+18delinsGAC	NP_001340694.1:n.311+16_311+18delinsGAC
XM_024452778.1:c.668+16_668+18delinsGAC	XP_024308546.1:n.668+16_668+18delinsGAC
XM_024452779.1:c.311+16_311+18delinsGAC	XP_024308547.1:n.311+16_311+18delinsGAC
NM_004304.5:c.3515+16_3515+18delinsGAC MANE Select	NP_004295.2:n.3515+16_3515+18delinsGAC
NM_001353765.2:c.311+16_311+18delinsGAC	NP_001340694.1:n.311+16_311+18delinsGAC