Canonical Allele Identifier: CA2658466787
Gene: ALK HGNC NCBI

Linked Data

gnomAD v4: 2-29328620-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328620G>T , CM000664.2:g.29328620G>T GRCh38
NC_000002.11:g.29551486G>T , CM000664.1:g.29551486G>T GRCh37
NC_000002.10:g.29404990G>T NCBI36
NG_009445.1:g.597947C>A , LRG_488:g.597947C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.1283-139C>A MANE Select ENSP00000373700.3:n.1283-139C>A
ENST00000389048.7:c.1283-139C>A ENSP00000373700.3:n.1283-139C>A
ENST00000618119.4:c.152-139C>A ENSP00000482733.1:n.152-139C>A
NM_004304.4:c.1283-139C>A NP_004295.2:n.1283-139C>A
XR_939920.1:n.817+111G>T
XR_939921.1:n.680+6092G>T
XR_001738688.2:n.2213-139C>A
XR_939920.2:n.707+111G>T
XR_939921.2:n.576+6092G>T
NM_004304.5:c.1283-139C>A MANE Select NP_004295.2:n.1283-139C>A
Search 100 bp 5'
Search 100 bp 3'