Canonical Allele Identifier: CA346473181

Gene: ALK

Linked Data

• ClinVar Variation Id: 538193
• ClinVar RCV Id: RCV000647395
• dbSNP Id: rs1553393928
• MyVariant Identifiers: chr2:g.29443691G>T (hg19) ; chr2:g.29220825G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220825G>T , CM000664.2:g.29220825G>T	GRCh38
NC_000002.11:g.29443691G>T , CM000664.1:g.29443691G>T	GRCh37
NC_000002.10:g.29297195G>T	NCBI36
NG_009445.1:g.705742C>A , LRG_488:g.705742C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3526C>A MANE Select	ENSP00000373700.3:p.His1176Asn
ENST00000431873.6:c.753C>A
ENST00000638605.1:n.403C>A
ENST00000642122.1:c.322C>A	ENSP00000493203.1:p.His108Asn
ENST00000389048.7:c.3526C>A	ENSP00000373700.3:p.His1176Asn
ENST00000431873.5:c.406C>A	ENSP00000414027.2:p.His136Asn
ENST00000618119.4:c.2395C>A	ENSP00000482733.1:p.His799Asn
NM_004304.4:c.3526C>A	NP_004295.2:p.His1176Asn
NM_001353765.1:c.322C>A	NP_001340694.1:p.His108Asn
XM_024452778.1:c.679C>A	XP_024308546.1:p.His227Asn
XM_024452779.1:c.322C>A	XP_024308547.1:p.His108Asn
NM_004304.5:c.3526C>A MANE Select	NP_004295.2:p.His1176Asn
NM_001353765.2:c.322C>A	NP_001340694.1:p.His108Asn