Canonical Allele Identifier: CA1241090503

Gene: ALK

Linked Data

• ClinVar Variation Id: 1951925
• ClinVar RCV Id: RCV002676596
• dbSNP Id: rs1385180881

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222330C>T , CM000664.2:g.29222330C>T	GRCh38
NC_000002.11:g.29445196C>T , CM000664.1:g.29445196C>T	GRCh37
NC_000002.10:g.29298700C>T	NCBI36
NG_009445.1:g.704237G>A , LRG_488:g.704237G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3515+14G>A MANE Select	ENSP00000373700.3:n.3515+14G>A
ENST00000431873.6:c.742+14G>A
ENST00000638605.1:n.392+14G>A
ENST00000642122.1:c.311+14G>A	ENSP00000493203.1:n.311+14G>A
ENST00000389048.7:c.3515+14G>A	ENSP00000373700.3:n.3515+14G>A
ENST00000431873.5:c.395+14G>A	ENSP00000414027.2:n.395+14G>A
ENST00000453137.1:c.209+14G>A	ENSP00000387488.1:n.209+14G>A
ENST00000618119.4:c.2384+14G>A	ENSP00000482733.1:n.2384+14G>A
NM_004304.4:c.3515+14G>A	NP_004295.2:n.3515+14G>A
NM_001353765.1:c.311+14G>A	NP_001340694.1:n.311+14G>A
XM_024452778.1:c.668+14G>A	XP_024308546.1:n.668+14G>A
XM_024452779.1:c.311+14G>A	XP_024308547.1:n.311+14G>A
NM_004304.5:c.3515+14G>A MANE Select	NP_004295.2:n.3515+14G>A
NM_001353765.2:c.311+14G>A	NP_001340694.1:n.311+14G>A