Canonical Allele Identifier: CA1241144924
Gene: ALK HGNC NCBI

Linked Data

dbSNP Id: rs1667349924

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328708G>C , CM000664.2:g.29328708G>C GRCh38
NC_000002.11:g.29551574G>C , CM000664.1:g.29551574G>C GRCh37
NC_000002.10:g.29405078G>C NCBI36
NG_009445.1:g.597859C>G , LRG_488:g.597859C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.1283-227C>G MANE Select ENSP00000373700.3:n.1283-227C>G
ENST00000389048.7:c.1283-227C>G ENSP00000373700.3:n.1283-227C>G
ENST00000618119.4:c.152-227C>G ENSP00000482733.1:n.152-227C>G
NM_004304.4:c.1283-227C>G NP_004295.2:n.1283-227C>G
XR_939920.1:n.817+199G>C
XR_939921.1:n.680+6180G>C
XR_001738688.2:n.2213-227C>G
XR_939920.2:n.707+199G>C
XR_939921.2:n.576+6180G>C
NM_004304.5:c.1283-227C>G MANE Select NP_004295.2:n.1283-227C>G