Canonical Allele Identifier: CA346474567

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29551333A>T (hg19) ; chr2:g.29328467A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29328467A>T , CM000664.2:g.29328467A>T	GRCh38
NC_000002.11:g.29551333A>T , CM000664.1:g.29551333A>T	GRCh37
NC_000002.10:g.29404837A>T	NCBI36
NG_009445.1:g.598100T>A , LRG_488:g.598100T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.1297T>A MANE Select	ENSP00000373700.3:p.Ser433Thr
ENST00000389048.7:c.1297T>A	ENSP00000373700.3:p.Ser433Thr
ENST00000618119.4:c.166T>A	ENSP00000482733.1:p.Ser56Thr
NM_004304.4:c.1297T>A	NP_004295.2:p.Ser433Thr
XR_939920.1:n.775A>T
XR_939921.1:n.680+5939A>T
XR_001738688.2:n.2227T>A
XR_939920.2:n.665A>T
XR_939921.2:n.576+5939A>T
NM_004304.5:c.1297T>A MANE Select	NP_004295.2:p.Ser433Thr