Canonical Allele Identifier: CA2698771469

Gene: ALK

Linked Data

• dbSNP Id: rs754701473

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220884G>T , CM000664.2:g.29220884G>T	GRCh38
NC_000002.11:g.29443750G>T , CM000664.1:g.29443750G>T	GRCh37
NC_000002.10:g.29297254G>T	NCBI36
NG_009445.1:g.705683C>A , LRG_488:g.705683C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3516-49C>A MANE Select	ENSP00000373700.3:n.3516-49C>A
ENST00000431873.6:c.743-49C>A
ENST00000638605.1:n.393-49C>A
ENST00000642122.1:c.312-49C>A	ENSP00000493203.1:n.312-49C>A
ENST00000389048.7:c.3516-49C>A	ENSP00000373700.3:n.3516-49C>A
ENST00000431873.5:c.396-49C>A	ENSP00000414027.2:n.396-49C>A
ENST00000453137.1:c.563C>A	ENSP00000387488.1:n.563C>A
ENST00000618119.4:c.2385-49C>A	ENSP00000482733.1:n.2385-49C>A
NM_004304.4:c.3516-49C>A	NP_004295.2:n.3516-49C>A
NM_001353765.1:c.312-49C>A	NP_001340694.1:n.312-49C>A
XM_024452778.1:c.669-49C>A	XP_024308546.1:n.669-49C>A
XM_024452779.1:c.312-49C>A	XP_024308547.1:n.312-49C>A
NM_004304.5:c.3516-49C>A MANE Select	NP_004295.2:n.3516-49C>A
NM_001353765.2:c.312-49C>A	NP_001340694.1:n.312-49C>A