Canonical Allele Identifier: CA425435995
Gene: ALK HGNC NCBI

Linked Data

dbSNP Id: rs2148178576
MyVariant Identifiers: chr2:g.29449885A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29227019A>G , CM000664.2:g.29227019A>G GRCh38
NC_000002.11:g.29449885A>G , CM000664.1:g.29449885A>G GRCh37
NC_000002.10:g.29303389A>G NCBI36
NG_009445.1:g.699548T>C , LRG_488:g.699548T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.2970T>C MANE Select ENSP00000373700.3:p.Cys990=
ENST00000431873.6:c.136T>C
ENST00000389048.7:c.2970T>C ENSP00000373700.3:p.Cys990=
ENST00000618119.4:c.1839T>C ENSP00000482733.1:p.Cys613=
NM_004304.4:c.2970T>C NP_004295.2:p.Cys990=
XM_024452778.1:c.123T>C XP_024308546.1:p.Cys41=
XR_001738688.2:n.3826T>C
NM_004304.5:c.2970T>C MANE Select NP_004295.2:p.Cys990=
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