Canonical Allele Identifier: CA346472608

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29320850C>G , CM000664.2:g.29320850C>G	GRCh38
NC_000002.11:g.29543716C>G , CM000664.1:g.29543716C>G	GRCh37
NC_000002.10:g.29397220C>G	NCBI36
NG_009445.1:g.605717G>C , LRG_488:g.605717G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004304.5:c.1447G>C MANE Select	NP_004295.2:p.Glu483Gln
ENST00000389048.8:c.1447G>C MANE Select	ENSP00000373700.3:p.Glu483Gln
NM_004304.4:c.1447G>C	NP_004295.2:p.Glu483Gln
ENST00000389048.7:c.1447G>C	ENSP00000373700.3:p.Glu483Gln
ENST00000618119.4:c.316G>C	ENSP00000482733.1:p.Glu106Gln
XR_001738688.2:n.2377G>C
XR_244977.3:n.560+877C>G
XR_244977.4:n.459+877C>G
XR_939920.1:n.584-629C>G
XR_939920.2:n.474-629C>G
XR_939921.1:n.572-629C>G
XR_939921.2:n.468-629C>G
XR_939922.1:n.563-629C>G
XR_939922.2:n.462-629C>G
XR_939923.1:n.563-629C>G
XR_939923.3:n.462-629C>G
XR_939924.1:n.563-629C>G
XR_939924.2:n.462-629C>G
XR_939925.1:n.560+877C>G
XR_939925.2:n.459+877C>G
XR_939926.1:n.560+877C>G
XR_939926.2:n.459+877C>G