Canonical Allele Identifier: CA531466855

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29209563dup , CM000664.2:g.29209563dup	GRCh38
NC_000002.11:g.29432429dup , CM000664.1:g.29432429dup	GRCh37
NC_000002.10:g.29285933dup	NCBI36
NG_009445.1:g.717024dup , LRG_488:g.717024dup

Transcript Alleles

HGVS	Amino-acid Change
NM_004304.5:c.3836+243dup MANE Select	NP_004295.2:n.3836+243dup
ENST00000389048.8:c.3836+243dup MANE Select	ENSP00000373700.3:n.3836+243dup
NM_001353765.1:c.632+243dup	NP_001340694.1:n.632+243dup
NM_001353765.2:c.632+243dup	NP_001340694.1:n.632+243dup
NM_004304.4:c.3836+243dup	NP_004295.2:n.3836+243dup
ENST00000389048.7:c.3836+243dup	ENSP00000373700.3:n.3836+243dup
ENST00000431873.5:c.716+243dup	ENSP00000414027.2:n.716+243dup
ENST00000431873.6:c.1063+243dup
ENST00000618119.4:c.2705+243dup	ENSP00000482733.1:n.2705+243dup
ENST00000638605.1:n.713+243dup
ENST00000642122.1:c.632+243dup	ENSP00000493203.1:n.632+243dup
XM_024452778.1:c.989+243dup	XP_024308546.1:n.989+243dup
XM_024452779.1:c.632+243dup	XP_024308547.1:n.632+243dup