Canonical Allele Identifier: CA1241144702

Gene: ALK

Linked Data

• dbSNP Id: rs1667342098

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29328491A>G , CM000664.2:g.29328491A>G	GRCh38
NC_000002.11:g.29551357A>G , CM000664.1:g.29551357A>G	GRCh37
NC_000002.10:g.29404861A>G	NCBI36
NG_009445.1:g.598076T>C , LRG_488:g.598076T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.1283-10T>C MANE Select	ENSP00000373700.3:n.1283-10T>C
ENST00000389048.7:c.1283-10T>C	ENSP00000373700.3:n.1283-10T>C
ENST00000618119.4:c.152-10T>C	ENSP00000482733.1:n.152-10T>C
NM_004304.4:c.1283-10T>C	NP_004295.2:n.1283-10T>C
XR_939920.1:n.799A>G
XR_939921.1:n.680+5963A>G
XR_001738688.2:n.2213-10T>C
XR_939920.2:n.689A>G
XR_939921.2:n.576+5963A>G
NM_004304.5:c.1283-10T>C MANE Select	NP_004295.2:n.1283-10T>C