Canonical Allele Identifier: CA346467975

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29449906A>T (hg19) ; chr2:g.29227040A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29227040A>T , CM000664.2:g.29227040A>T	GRCh38
NC_000002.11:g.29449906A>T , CM000664.1:g.29449906A>T	GRCh37
NC_000002.10:g.29303410A>T	NCBI36
NG_009445.1:g.699527T>A , LRG_488:g.699527T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.2949T>A MANE Select	ENSP00000373700.3:p.His983Gln
ENST00000431873.6:c.115T>A
ENST00000389048.7:c.2949T>A	ENSP00000373700.3:p.His983Gln
ENST00000618119.4:c.1818T>A	ENSP00000482733.1:p.His606Gln
NM_004304.4:c.2949T>A	NP_004295.2:p.His983Gln
XM_024452778.1:c.102T>A	XP_024308546.1:p.His34Gln
XR_001738688.2:n.3805T>A
NM_004304.5:c.2949T>A MANE Select	NP_004295.2:p.His983Gln