Canonical Allele Identifier: CA2658466662
Gene: ALK HGNC NCBI

Linked Data

gnomAD v4: 2-29328487-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328487G>A , CM000664.2:g.29328487G>A GRCh38
NC_000002.11:g.29551353G>A , CM000664.1:g.29551353G>A GRCh37
NC_000002.10:g.29404857G>A NCBI36
NG_009445.1:g.598080C>T , LRG_488:g.598080C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.1283-6C>T MANE Select ENSP00000373700.3:n.1283-6C>T
ENST00000389048.7:c.1283-6C>T ENSP00000373700.3:n.1283-6C>T
ENST00000618119.4:c.152-6C>T ENSP00000482733.1:n.152-6C>T
NM_004304.4:c.1283-6C>T NP_004295.2:n.1283-6C>T
XR_939920.1:n.795G>A
XR_939921.1:n.680+5959G>A
XR_001738688.2:n.2213-6C>T
XR_939920.2:n.685G>A
XR_939921.2:n.576+5959G>A
NM_004304.5:c.1283-6C>T MANE Select NP_004295.2:n.1283-6C>T
Search 100 bp 5'
Search 100 bp 3'