Canonical Allele Identifier: CA2658467202

Gene: ALK

Linked Data

• gnomAD v4: 2-29328272-ATGCCTGGGATAATGGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29328273_29328288del , CM000664.2:g.29328273_29328288del	GRCh38
NC_000002.11:g.29551139_29551154del , CM000664.1:g.29551139_29551154del	GRCh37
NC_000002.10:g.29404643_29404658del	NCBI36
NG_009445.1:g.598279_598294del , LRG_488:g.598279_598294del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.1414+62_1414+77del MANE Select	ENSP00000373700.3:n.1414+62_1414+77del
ENST00000389048.7:c.1414+62_1414+77del	ENSP00000373700.3:n.1414+62_1414+77del
ENST00000618119.4:c.283+62_283+77del	ENSP00000482733.1:n.283+62_283+77del
NM_004304.4:c.1414+62_1414+77del	NP_004295.2:n.1414+62_1414+77del
XR_939920.1:n.693-112_693-97del
XR_939921.1:n.680+5745_680+5760del
XR_001738688.2:n.2344+62_2344+77del
XR_244977.4:n.1765_1780del
XR_939920.2:n.583-112_583-97del
XR_939921.2:n.576+5745_576+5760del
XR_939922.2:n.1805_1820del
NM_004304.5:c.1414+62_1414+77del MANE Select	NP_004295.2:n.1414+62_1414+77del