Canonical Allele Identifier: CA346473165

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29443685T>C (hg19) ; chr2:g.29220819T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220819T>C , CM000664.2:g.29220819T>C	GRCh38
NC_000002.11:g.29443685T>C , CM000664.1:g.29443685T>C	GRCh37
NC_000002.10:g.29297189T>C	NCBI36
NG_009445.1:g.705748A>G , LRG_488:g.705748A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3532A>G MANE Select	ENSP00000373700.3:p.Asn1178Asp
ENST00000431873.6:c.759A>G
ENST00000638605.1:n.409A>G
ENST00000642122.1:c.328A>G	ENSP00000493203.1:p.Asn110Asp
ENST00000389048.7:c.3532A>G	ENSP00000373700.3:p.Asn1178Asp
ENST00000431873.5:c.412A>G	ENSP00000414027.2:p.Asn138Asp
ENST00000618119.4:c.2401A>G	ENSP00000482733.1:p.Asn801Asp
NM_004304.4:c.3532A>G	NP_004295.2:p.Asn1178Asp
NM_001353765.1:c.328A>G	NP_001340694.1:p.Asn110Asp
XM_024452778.1:c.685A>G	XP_024308546.1:p.Asn229Asp
XM_024452779.1:c.328A>G	XP_024308547.1:p.Asn110Asp
NM_004304.5:c.3532A>G MANE Select	NP_004295.2:p.Asn1178Asp
NM_001353765.2:c.328A>G	NP_001340694.1:p.Asn110Asp