Canonical Allele Identifier: CA1594863
Gene: ALK HGNC NCBI

Linked Data

dbSNP Id: rs201887630
ExAC: 2:29940410 G / C
gnomAD v2: 2-29940410-G-C
MyVariant Identifiers: chr2:g.29940410G>C (hg19) chr2:g.29717544G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29717544G>C , CM000664.2:g.29717544G>C GRCh38
NC_000002.11:g.29940410G>C , CM000664.1:g.29940410G>C GRCh37
NC_000002.10:g.29793914G>C NCBI36
NG_009445.1:g.209023C>G , LRG_488:g.209023C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.787+34C>G MANE Select ENSP00000373700.3:n.787+34C>G
ENST00000389048.7:c.787+34C>G ENSP00000373700.3:n.787+34C>G
ENST00000618119.4:c.-345+34C>G ENSP00000482733.1:n.-345+34C>G
NM_004304.4:c.787+34C>G NP_004295.2:n.787+34C>G
XR_001738688.2:n.1717+34C>G
NM_004304.5:c.787+34C>G MANE Select NP_004295.2:n.787+34C>G
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