Canonical Allele Identifier: CA425435942
Gene: ALK HGNC NCBI

Linked Data

gnomAD v4: 2-29226965-A-G
MyVariant Identifiers: chr2:g.29449831A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29226965A>G , CM000664.2:g.29226965A>G GRCh38
NC_000002.11:g.29449831A>G , CM000664.1:g.29449831A>G GRCh37
NC_000002.10:g.29303335A>G NCBI36
NG_009445.1:g.699602T>C , LRG_488:g.699602T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.3024T>C MANE Select ENSP00000373700.3:p.Cys1008=
ENST00000431873.6:c.190T>C
ENST00000389048.7:c.3024T>C ENSP00000373700.3:p.Cys1008=
ENST00000618119.4:c.1893T>C ENSP00000482733.1:p.Cys631=
NM_004304.4:c.3024T>C NP_004295.2:p.Cys1008=
XM_024452778.1:c.177T>C XP_024308546.1:p.Cys59=
XR_001738688.2:n.3880T>C
NM_004304.5:c.3024T>C MANE Select NP_004295.2:p.Cys1008=
Search 100 bp 5'
Search 100 bp 3'