Canonical Allele Identifier: CA346468104

Gene: ALK

Linked Data

• ClinVar Variation Id: 844656
• ClinVar RCV Id: RCV001047565
• dbSNP Id: rs1664022542
• MyVariant Identifiers: chr2:g.29449929G>A (hg19) ; chr2:g.29227063G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29227063G>A , CM000664.2:g.29227063G>A	GRCh38
NC_000002.11:g.29449929G>A , CM000664.1:g.29449929G>A	GRCh37
NC_000002.10:g.29303433G>A	NCBI36
NG_009445.1:g.699504C>T , LRG_488:g.699504C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.2926C>T MANE Select	ENSP00000373700.3:p.His976Tyr
ENST00000431873.6:c.92C>T
ENST00000389048.7:c.2926C>T	ENSP00000373700.3:p.His976Tyr
ENST00000618119.4:c.1795C>T	ENSP00000482733.1:p.His599Tyr
NM_004304.4:c.2926C>T	NP_004295.2:p.His976Tyr
XM_024452778.1:c.79C>T	XP_024308546.1:p.His27Tyr
XR_001738688.2:n.3782C>T
NM_004304.5:c.2926C>T MANE Select	NP_004295.2:p.His976Tyr