Canonical Allele Identifier: CA767606135
Gene: ALK HGNC NCBI

Linked Data

dbSNP Id: rs1204400971
gnomAD v4: 2-29717523-C-T
MyVariant Identifiers: chr2:g.29940389C>T (hg19) chr2:g.29717523C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29717523C>T , CM000664.2:g.29717523C>T GRCh38
NC_000002.11:g.29940389C>T , CM000664.1:g.29940389C>T GRCh37
NC_000002.10:g.29793893C>T NCBI36
NG_009445.1:g.209044G>A , LRG_488:g.209044G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.787+55G>A MANE Select ENSP00000373700.3:n.787+55G>A
ENST00000389048.7:c.787+55G>A ENSP00000373700.3:n.787+55G>A
ENST00000618119.4:c.-345+55G>A ENSP00000482733.1:n.-345+55G>A
NM_004304.4:c.787+55G>A NP_004295.2:n.787+55G>A
XR_001738688.2:n.1717+55G>A
NM_004304.5:c.787+55G>A MANE Select NP_004295.2:n.787+55G>A
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