Canonical Allele Identifier: CA346473164

Gene: ALK

Linked Data

• dbSNP Id: rs2148166684
• MyVariant Identifiers: chr2:g.29443685T>A (hg19) ; chr2:g.29220819T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3532A>T MANE Select	ENSP00000373700.3:p.Asn1178Tyr
ENST00000431873.6:c.759A>T
ENST00000638605.1:n.409A>T
ENST00000642122.1:c.328A>T	ENSP00000493203.1:p.Asn110Tyr
ENST00000389048.7:c.3532A>T	ENSP00000373700.3:p.Asn1178Tyr
ENST00000431873.5:c.412A>T	ENSP00000414027.2:p.Asn138Tyr
ENST00000618119.4:c.2401A>T	ENSP00000482733.1:p.Asn801Tyr
NM_004304.4:c.3532A>T	NP_004295.2:p.Asn1178Tyr
NM_001353765.1:c.328A>T	NP_001340694.1:p.Asn110Tyr
XM_024452778.1:c.685A>T	XP_024308546.1:p.Asn229Tyr
XM_024452779.1:c.328A>T	XP_024308547.1:p.Asn110Tyr
NM_004304.5:c.3532A>T MANE Select	NP_004295.2:p.Asn1178Tyr
NM_001353765.2:c.328A>T	NP_001340694.1:p.Asn110Tyr