Canonical Allele Identifier: CA346467621

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29449834G>T (hg19) ; chr2:g.29226968G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29226968G>T , CM000664.2:g.29226968G>T	GRCh38
NC_000002.11:g.29449834G>T , CM000664.1:g.29449834G>T	GRCh37
NC_000002.10:g.29303338G>T	NCBI36
NG_009445.1:g.699599C>A , LRG_488:g.699599C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3021C>A MANE Select	ENSP00000373700.3:p.Phe1007Leu
ENST00000431873.6:c.187C>A
ENST00000389048.7:c.3021C>A	ENSP00000373700.3:p.Phe1007Leu
ENST00000618119.4:c.1890C>A	ENSP00000482733.1:p.Phe630Leu
NM_004304.4:c.3021C>A	NP_004295.2:p.Phe1007Leu
XM_024452778.1:c.174C>A	XP_024308546.1:p.Phe58Leu
XR_001738688.2:n.3877C>A
NM_004304.5:c.3021C>A MANE Select	NP_004295.2:p.Phe1007Leu