Canonical Allele Identifier: CA346467624

Gene: ALK

Linked Data

• dbSNP Id: rs1558626190
• MyVariant Identifiers: chr2:g.29449835A>T (hg19) ; chr2:g.29226969A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29226969A>T , CM000664.2:g.29226969A>T	GRCh38
NC_000002.11:g.29449835A>T , CM000664.1:g.29449835A>T	GRCh37
NC_000002.10:g.29303339A>T	NCBI36
NG_009445.1:g.699598T>A , LRG_488:g.699598T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3020T>A MANE Select	ENSP00000373700.3:p.Phe1007Tyr
ENST00000431873.6:c.186T>A
ENST00000389048.7:c.3020T>A	ENSP00000373700.3:p.Phe1007Tyr
ENST00000618119.4:c.1889T>A	ENSP00000482733.1:p.Phe630Tyr
NM_004304.4:c.3020T>A	NP_004295.2:p.Phe1007Tyr
XM_024452778.1:c.173T>A	XP_024308546.1:p.Phe58Tyr
XR_001738688.2:n.3876T>A
NM_004304.5:c.3020T>A MANE Select	NP_004295.2:p.Phe1007Tyr