Canonical Allele Identifier: CA346468140

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29449937A>G (hg19) ; chr2:g.29227071A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29227071A>G , CM000664.2:g.29227071A>G	GRCh38
NC_000002.11:g.29449937A>G , CM000664.1:g.29449937A>G	GRCh37
NC_000002.10:g.29303441A>G	NCBI36
NG_009445.1:g.699496T>C , LRG_488:g.699496T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.2918T>C MANE Select	ENSP00000373700.3:p.Met973Thr
ENST00000431873.6:c.84T>C
ENST00000389048.7:c.2918T>C	ENSP00000373700.3:p.Met973Thr
ENST00000618119.4:c.1787T>C	ENSP00000482733.1:p.Met596Thr
NM_004304.4:c.2918T>C	NP_004295.2:p.Met973Thr
XM_024452778.1:c.71T>C	XP_024308546.1:p.Met24Thr
XR_001738688.2:n.3774T>C
NM_004304.5:c.2918T>C MANE Select	NP_004295.2:p.Met973Thr