Canonical Allele Identifier: CA2576925270

Gene: ALK

Linked Data

• gnomAD v4: 2-29222272-C-CTGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222273_29222276dup , CM000664.2:g.29222273_29222276dup	GRCh38
NC_000002.11:g.29445139_29445142dup , CM000664.1:g.29445139_29445142dup	GRCh37
NC_000002.10:g.29298643_29298646dup	NCBI36
NG_009445.1:g.704291_704294dup , LRG_488:g.704291_704294dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3515+68_3515+71dup MANE Select	ENSP00000373700.3:n.3515+68_3515+71dup
ENST00000431873.6:c.742+68_742+71dup
ENST00000638605.1:n.392+68_392+71dup
ENST00000642122.1:c.311+68_311+71dup	ENSP00000493203.1:n.311+68_311+71dup
ENST00000389048.7:c.3515+68_3515+71dup	ENSP00000373700.3:n.3515+68_3515+71dup
ENST00000431873.5:c.395+68_395+71dup	ENSP00000414027.2:n.395+68_395+71dup
ENST00000453137.1:c.209+68_209+71dup	ENSP00000387488.1:n.209+68_209+71dup
ENST00000618119.4:c.2384+68_2384+71dup	ENSP00000482733.1:n.2384+68_2384+71dup
NM_004304.4:c.3515+68_3515+71dup	NP_004295.2:n.3515+68_3515+71dup
NM_001353765.1:c.311+68_311+71dup	NP_001340694.1:n.311+68_311+71dup
XM_024452778.1:c.668+68_668+71dup	XP_024308546.1:n.668+68_668+71dup
XM_024452779.1:c.311+68_311+71dup	XP_024308547.1:n.311+68_311+71dup
NM_004304.5:c.3515+68_3515+71dup MANE Select	NP_004295.2:n.3515+68_3515+71dup
NM_001353765.2:c.311+68_311+71dup	NP_001340694.1:n.311+68_311+71dup