Canonical Allele Identifier: CA1241144720
Gene: ALK HGNC NCBI

Linked Data

dbSNP Id: rs1667343019
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328510G>C , CM000664.2:g.29328510G>C GRCh38
NC_000002.11:g.29551376G>C , CM000664.1:g.29551376G>C GRCh37
NC_000002.10:g.29404880G>C NCBI36
NG_009445.1:g.598057C>G , LRG_488:g.598057C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.1283-29C>G MANE Select ENSP00000373700.3:n.1283-29C>G
ENST00000389048.7:c.1283-29C>G ENSP00000373700.3:n.1283-29C>G
ENST00000618119.4:c.152-29C>G ENSP00000482733.1:n.152-29C>G
NM_004304.4:c.1283-29C>G NP_004295.2:n.1283-29C>G
XR_939920.1:n.817+1G>C
XR_939921.1:n.680+5982G>C
XR_001738688.2:n.2213-29C>G
XR_939920.2:n.707+1G>C
XR_939921.2:n.576+5982G>C
NM_004304.5:c.1283-29C>G MANE Select NP_004295.2:n.1283-29C>G
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