Canonical Allele Identifier: CA346468106
Gene: ALK HGNC NCBI

Linked Data

dbSNP Id: rs1664022542
MyVariant Identifiers: chr2:g.29449929G>C (hg19) chr2:g.29227063G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29227063G>C , CM000664.2:g.29227063G>C GRCh38
NC_000002.11:g.29449929G>C , CM000664.1:g.29449929G>C GRCh37
NC_000002.10:g.29303433G>C NCBI36
NG_009445.1:g.699504C>G , LRG_488:g.699504C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.2926C>G MANE Select ENSP00000373700.3:p.His976Asp
ENST00000431873.6:c.92C>G
ENST00000389048.7:c.2926C>G ENSP00000373700.3:p.His976Asp
ENST00000618119.4:c.1795C>G ENSP00000482733.1:p.His599Asp
NM_004304.4:c.2926C>G NP_004295.2:p.His976Asp
XM_024452778.1:c.79C>G XP_024308546.1:p.His27Asp
XR_001738688.2:n.3782C>G
NM_004304.5:c.2926C>G MANE Select NP_004295.2:p.His976Asp
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