Canonical Allele Identifier: CA1241144417
Gene: ALK HGNC NCBI

Linked Data

dbSNP Id: rs1667334461
gnomAD v4: 2-29328290-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328290A>G , CM000664.2:g.29328290A>G GRCh38
NC_000002.11:g.29551156A>G , CM000664.1:g.29551156A>G GRCh37
NC_000002.10:g.29404660A>G NCBI36
NG_009445.1:g.598277T>C , LRG_488:g.598277T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.1414+60T>C MANE Select ENSP00000373700.3:n.1414+60T>C
ENST00000389048.7:c.1414+60T>C ENSP00000373700.3:n.1414+60T>C
ENST00000618119.4:c.283+60T>C ENSP00000482733.1:n.283+60T>C
NM_004304.4:c.1414+60T>C NP_004295.2:n.1414+60T>C
XR_939920.1:n.693-95A>G
XR_939921.1:n.680+5762A>G
XR_001738688.2:n.2344+60T>C
XR_244977.4:n.1782A>G
XR_939920.2:n.583-95A>G
XR_939921.2:n.576+5762A>G
XR_939922.2:n.1822A>G
NM_004304.5:c.1414+60T>C MANE Select NP_004295.2:n.1414+60T>C