Canonical Allele Identifier: CA2576925709

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29328293_29328295del , CM000664.2:g.29328293_29328295del	GRCh38
NC_000002.11:g.29551159_29551161del , CM000664.1:g.29551159_29551161del	GRCh37
NC_000002.10:g.29404663_29404665del	NCBI36
NG_009445.1:g.598272_598274del , LRG_488:g.598272_598274del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.1414+55_1414+57del MANE Select	ENSP00000373700.3:n.1414+55_1414+57del
ENST00000389048.7:c.1414+55_1414+57del	ENSP00000373700.3:n.1414+55_1414+57del
ENST00000618119.4:c.283+55_283+57del	ENSP00000482733.1:n.283+55_283+57del
NM_004304.4:c.1414+55_1414+57del	NP_004295.2:n.1414+55_1414+57del
XR_939920.1:n.693-92_693-90del
XR_939921.1:n.680+5765_680+5767del
XR_001738688.2:n.2344+55_2344+57del
XR_244977.4:n.1785_1787del
XR_939920.2:n.583-92_583-90del
XR_939921.2:n.576+5765_576+5767del
XR_939922.2:n.1825_1827del
NM_004304.5:c.1414+55_1414+57del MANE Select	NP_004295.2:n.1414+55_1414+57del