Canonical Allele Identifier: CA346467618

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29449833A>T (hg19) ; chr2:g.29226967A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29226967A>T , CM000664.2:g.29226967A>T	GRCh38
NC_000002.11:g.29449833A>T , CM000664.1:g.29449833A>T	GRCh37
NC_000002.10:g.29303337A>T	NCBI36
NG_009445.1:g.699600T>A , LRG_488:g.699600T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3022T>A MANE Select	ENSP00000373700.3:p.Cys1008Ser
ENST00000431873.6:c.188T>A
ENST00000389048.7:c.3022T>A	ENSP00000373700.3:p.Cys1008Ser
ENST00000618119.4:c.1891T>A	ENSP00000482733.1:p.Cys631Ser
NM_004304.4:c.3022T>A	NP_004295.2:p.Cys1008Ser
XM_024452778.1:c.175T>A	XP_024308546.1:p.Cys59Ser
XR_001738688.2:n.3878T>A
NM_004304.5:c.3022T>A MANE Select	NP_004295.2:p.Cys1008Ser