Canonical Allele Identifier: CA346467813

Gene: ALK

Linked Data

• dbSNP Id: rs2148178571
• MyVariant Identifiers: chr2:g.29449884C>G (hg19) ; chr2:g.29227018C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29227018C>G , CM000664.2:g.29227018C>G	GRCh38
NC_000002.11:g.29449884C>G , CM000664.1:g.29449884C>G	GRCh37
NC_000002.10:g.29303388C>G	NCBI36
NG_009445.1:g.699549G>C , LRG_488:g.699549G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.2971G>C MANE Select	ENSP00000373700.3:p.Glu991Gln
ENST00000431873.6:c.137G>C
ENST00000389048.7:c.2971G>C	ENSP00000373700.3:p.Glu991Gln
ENST00000618119.4:c.1840G>C	ENSP00000482733.1:p.Glu614Gln
NM_004304.4:c.2971G>C	NP_004295.2:p.Glu991Gln
XM_024452778.1:c.124G>C	XP_024308546.1:p.Glu42Gln
XR_001738688.2:n.3827G>C
NM_004304.5:c.2971G>C MANE Select	NP_004295.2:p.Glu991Gln