Canonical Allele Identifier: CA346474559

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29551332G>C (hg19) ; chr2:g.29328466G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29328466G>C , CM000664.2:g.29328466G>C	GRCh38
NC_000002.11:g.29551332G>C , CM000664.1:g.29551332G>C	GRCh37
NC_000002.10:g.29404836G>C	NCBI36
NG_009445.1:g.598101C>G , LRG_488:g.598101C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.1298C>G MANE Select	ENSP00000373700.3:p.Ser433Cys
ENST00000389048.7:c.1298C>G	ENSP00000373700.3:p.Ser433Cys
ENST00000618119.4:c.167C>G	ENSP00000482733.1:p.Ser56Cys
NM_004304.4:c.1298C>G	NP_004295.2:p.Ser433Cys
XR_939920.1:n.774G>C
XR_939921.1:n.680+5938G>C
XR_001738688.2:n.2228C>G
XR_939920.2:n.664G>C
XR_939921.2:n.576+5938G>C
NM_004304.5:c.1298C>G MANE Select	NP_004295.2:p.Ser433Cys