Canonical Allele Identifier: CA1241144992
Gene: ALK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328796T= , CM000664.2:g.29328796T= GRCh38
NC_000002.11:g.29551662T= , CM000664.1:g.29551662T= GRCh37
NC_000002.10:g.29405166T= NCBI36
NG_009445.1:g.597771A= , LRG_488:g.597771A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.1283-315A= MANE Select ENSP00000373700.3:n.1283-315A=
ENST00000389048.7:c.1283-315A= ENSP00000373700.3:n.1283-315A=
ENST00000618119.4:c.152-315A= ENSP00000482733.1:n.152-315A=
NM_004304.4:c.1283-315A= NP_004295.2:n.1283-315A=
XR_939920.1:n.818-129T=
XR_939921.1:n.680+6268T=
XR_001738688.2:n.2213-315A=
XR_939920.2:n.708-129T=
XR_939921.2:n.576+6268T=
NM_004304.5:c.1283-315A= MANE Select NP_004295.2:n.1283-315A=
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