Canonical Allele Identifier: CA346467620

Gene: ALK

Linked Data

• dbSNP Id: rs2148178438
• MyVariant Identifiers: chr2:g.29449834G>C (hg19) ; chr2:g.29226968G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29226968G>C , CM000664.2:g.29226968G>C	GRCh38
NC_000002.11:g.29449834G>C , CM000664.1:g.29449834G>C	GRCh37
NC_000002.10:g.29303338G>C	NCBI36
NG_009445.1:g.699599C>G , LRG_488:g.699599C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3021C>G MANE Select	ENSP00000373700.3:p.Phe1007Leu
ENST00000431873.6:c.187C>G
ENST00000389048.7:c.3021C>G	ENSP00000373700.3:p.Phe1007Leu
ENST00000618119.4:c.1890C>G	ENSP00000482733.1:p.Phe630Leu
NM_004304.4:c.3021C>G	NP_004295.2:p.Phe1007Leu
XM_024452778.1:c.174C>G	XP_024308546.1:p.Phe58Leu
XR_001738688.2:n.3877C>G
NM_004304.5:c.3021C>G MANE Select	NP_004295.2:p.Phe1007Leu