Canonical Allele Identifier: CA1241144709

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29328496G= , CM000664.2:g.29328496G=	GRCh38
NC_000002.11:g.29551362G= , CM000664.1:g.29551362G=	GRCh37
NC_000002.10:g.29404866G=	NCBI36
NG_009445.1:g.598071C= , LRG_488:g.598071C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.1283-15C= MANE Select	ENSP00000373700.3:n.1283-15C=
ENST00000389048.7:c.1283-15C=	ENSP00000373700.3:n.1283-15C=
ENST00000618119.4:c.152-15C=	ENSP00000482733.1:n.152-15C=
NM_004304.4:c.1283-15C=	NP_004295.2:n.1283-15C=
XR_939920.1:n.804G=
XR_939921.1:n.680+5968G=
XR_001738688.2:n.2213-15C=
XR_939920.2:n.694G=
XR_939921.2:n.576+5968G=
NM_004304.5:c.1283-15C= MANE Select	NP_004295.2:n.1283-15C=