Canonical Allele Identifier: CA1241090590

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222496_29222498delinsCAA , CM000664.2:g.29222496_29222498delinsCAA	GRCh38
NC_000002.11:g.29445362_29445364delinsCAA , CM000664.1:g.29445362_29445364delinsCAA	GRCh37
NC_000002.10:g.29298866_29298868delinsCAA	NCBI36
NG_009445.1:g.704069_704071delinsTTG , LRG_488:g.704069_704071delinsTTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.3450+19_3450+21delinsTTG MANE Select	ENSP00000373700.3:n.3450+19_3450+21delins...
ENST00000431873.6:c.677+19_677+21delinsTTG
ENST00000638605.1:n.327+19_327+21delinsTTG
ENST00000642122.1:c.246+19_246+21delinsTTG	ENSP00000493203.1:n.246+19_246+21delinsTT...
ENST00000389048.7:c.3450+19_3450+21delinsTTG	ENSP00000373700.3:n.3450+19_3450+21delins...
ENST00000431873.5:c.330+19_330+21delinsTTG	ENSP00000414027.2:n.330+19_330+21delinsTT...
ENST00000453137.1:c.144+19_144+21delinsTTG	ENSP00000387488.1:n.144+19_144+21delinsTT...
ENST00000618119.4:c.2319+19_2319+21delinsTTG	ENSP00000482733.1:n.2319+19_2319+21delins...
NM_004304.4:c.3450+19_3450+21delinsTTG	NP_004295.2:n.3450+19_3450+21delinsTTG
NM_001353765.1:c.246+19_246+21delinsTTG	NP_001340694.1:n.246+19_246+21delinsTTG
XM_024452778.1:c.603+19_603+21delinsTTG	XP_024308546.1:n.603+19_603+21delinsTTG
XM_024452779.1:c.246+19_246+21delinsTTG	XP_024308547.1:n.246+19_246+21delinsTTG
NM_004304.5:c.3450+19_3450+21delinsTTG MANE Select	NP_004295.2:n.3450+19_3450+21delinsTTG
NM_001353765.2:c.246+19_246+21delinsTTG	NP_001340694.1:n.246+19_246+21delinsTTG