Canonical Allele Identifier: CA425619408

Gene: ALK

Linked Data

• ClinVar Variation Id: 538291
• ClinVar RCV Id: RCV000647500 ; RCV002458115
• dbSNP Id: rs1553393901
• MyVariant Identifiers: chr2:g.29443641C>A (hg19) ; chr2:g.29220775C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220775C>A , CM000664.2:g.29220775C>A	GRCh38
NC_000002.11:g.29443641C>A , CM000664.1:g.29443641C>A	GRCh37
NC_000002.10:g.29297145C>A	NCBI36
NG_009445.1:g.705792G>T , LRG_488:g.705792G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3576G>T MANE Select	ENSP00000373700.3:p.Arg1192=
ENST00000431873.6:c.803G>T
ENST00000638605.1:n.453G>T
ENST00000642122.1:c.372G>T	ENSP00000493203.1:p.Arg124=
ENST00000389048.7:c.3576G>T	ENSP00000373700.3:p.Arg1192=
ENST00000431873.5:c.456G>T	ENSP00000414027.2:p.Arg152=
ENST00000618119.4:c.2445G>T	ENSP00000482733.1:p.Arg815=
NM_004304.4:c.3576G>T	NP_004295.2:p.Arg1192=
NM_001353765.1:c.372G>T	NP_001340694.1:p.Arg124=
XM_024452778.1:c.729G>T	XP_024308546.1:p.Arg243=
XM_024452779.1:c.372G>T	XP_024308547.1:p.Arg124=
NM_004304.5:c.3576G>T MANE Select	NP_004295.2:p.Arg1192=
NM_001353765.2:c.372G>T	NP_001340694.1:p.Arg124=