Canonical Allele Identifier: CA2573134528

Gene: ALK

Linked Data

• ClinVar Variation Id: 1614570
• ClinVar RCV Id: RCV002078710
• dbSNP Id: rs2148166225

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220697C>G , CM000664.2:g.29220697C>G	GRCh38
NC_000002.11:g.29443563C>G , CM000664.1:g.29443563C>G	GRCh37
NC_000002.10:g.29297067C>G	NCBI36
NG_009445.1:g.705870G>C , LRG_488:g.705870G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3645+9G>C MANE Select	ENSP00000373700.3:n.3645+9G>C
ENST00000431873.6:c.872+9G>C
ENST00000638605.1:n.522+9G>C
ENST00000642122.1:c.441+9G>C	ENSP00000493203.1:n.441+9G>C
ENST00000389048.7:c.3645+9G>C	ENSP00000373700.3:n.3645+9G>C
ENST00000431873.5:c.525+9G>C	ENSP00000414027.2:n.525+9G>C
ENST00000618119.4:c.2514+9G>C	ENSP00000482733.1:n.2514+9G>C
NM_004304.4:c.3645+9G>C	NP_004295.2:n.3645+9G>C
NM_001353765.1:c.441+9G>C	NP_001340694.1:n.441+9G>C
XM_024452778.1:c.798+9G>C	XP_024308546.1:n.798+9G>C
XM_024452779.1:c.441+9G>C	XP_024308547.1:n.441+9G>C
NM_004304.5:c.3645+9G>C MANE Select	NP_004295.2:n.3645+9G>C
NM_001353765.2:c.441+9G>C	NP_001340694.1:n.441+9G>C