Canonical Allele Identifier: CA2581758825
Gene: ALK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328295G>C , CM000664.2:g.29328295G>C GRCh38
NC_000002.11:g.29551161G>C , CM000664.1:g.29551161G>C GRCh37
NC_000002.10:g.29404665G>C NCBI36
NG_009445.1:g.598272C>G , LRG_488:g.598272C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.1414+55C>G MANE Select ENSP00000373700.3:n.1414+55C>G
ENST00000389048.7:c.1414+55C>G ENSP00000373700.3:n.1414+55C>G
ENST00000618119.4:c.283+55C>G ENSP00000482733.1:n.283+55C>G
NM_004304.4:c.1414+55C>G NP_004295.2:n.1414+55C>G
XR_939920.1:n.693-90G>C
XR_939921.1:n.680+5767G>C
XR_001738688.2:n.2344+55C>G
XR_244977.4:n.1787G>C
XR_939920.2:n.583-90G>C
XR_939921.2:n.576+5767G>C
XR_939922.2:n.1827G>C
NM_004304.5:c.1414+55C>G MANE Select NP_004295.2:n.1414+55C>G