Canonical Allele Identifier: CA2749326737

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220677_29220679dup , CM000664.2:g.29220677_29220679dup	GRCh38
NC_000002.11:g.29443543_29443545dup , CM000664.1:g.29443543_29443545dup	GRCh37
NC_000002.10:g.29297047_29297049dup	NCBI36
NG_009445.1:g.705893_705895dup , LRG_488:g.705893_705895dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3645+32_3645+34dup MANE Select	ENSP00000373700.3:n.3645+32_3645+34dup
ENST00000431873.6:c.872+32_872+34dup
ENST00000638605.1:n.522+32_522+34dup
ENST00000642122.1:c.441+32_441+34dup	ENSP00000493203.1:n.441+32_441+34dup
ENST00000389048.7:c.3645+32_3645+34dup	ENSP00000373700.3:n.3645+32_3645+34dup
ENST00000431873.5:c.525+32_525+34dup	ENSP00000414027.2:n.525+32_525+34dup
ENST00000618119.4:c.2514+32_2514+34dup	ENSP00000482733.1:n.2514+32_2514+34dup
NM_004304.4:c.3645+32_3645+34dup	NP_004295.2:n.3645+32_3645+34dup
NM_001353765.1:c.441+32_441+34dup	NP_001340694.1:n.441+32_441+34dup
XM_024452778.1:c.798+32_798+34dup	XP_024308546.1:n.798+32_798+34dup
XM_024452779.1:c.441+32_441+34dup	XP_024308547.1:n.441+32_441+34dup
NM_004304.5:c.3645+32_3645+34dup MANE Select	NP_004295.2:n.3645+32_3645+34dup
NM_001353765.2:c.441+32_441+34dup	NP_001340694.1:n.441+32_441+34dup