Canonical Allele Identifier: CA425619397

Gene: ALK

Linked Data

• ClinVar Variation Id: 1732959
• ClinVar RCV Id: RCV002455117
• dbSNP Id: rs1418386125
• MyVariant Identifiers: chr2:g.29443629C>T (hg19) ; chr2:g.29220763C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220763C>T , CM000664.2:g.29220763C>T	GRCh38
NC_000002.11:g.29443629C>T , CM000664.1:g.29443629C>T	GRCh37
NC_000002.10:g.29297133C>T	NCBI36
NG_009445.1:g.705804G>A , LRG_488:g.705804G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3588G>A MANE Select	ENSP00000373700.3:p.Leu1196=
ENST00000431873.6:c.815G>A
ENST00000638605.1:n.465G>A
ENST00000642122.1:c.384G>A	ENSP00000493203.1:p.Leu128=
ENST00000389048.7:c.3588G>A	ENSP00000373700.3:p.Leu1196=
ENST00000431873.5:c.468G>A	ENSP00000414027.2:p.Leu156=
ENST00000618119.4:c.2457G>A	ENSP00000482733.1:p.Leu819=
NM_004304.4:c.3588G>A	NP_004295.2:p.Leu1196=
NM_001353765.1:c.384G>A	NP_001340694.1:p.Leu128=
XM_024452778.1:c.741G>A	XP_024308546.1:p.Leu247=
XM_024452779.1:c.384G>A	XP_024308547.1:p.Leu128=
NM_004304.5:c.3588G>A MANE Select	NP_004295.2:p.Leu1196=
NM_001353765.2:c.384G>A	NP_001340694.1:p.Leu128=