Canonical Allele Identifier: CA346473187

Gene: ALK

Linked Data

• dbSNP Id: rs2148166712
• MyVariant Identifiers: chr2:g.29443694T>C (hg19) ; chr2:g.29220828T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220828T>C , CM000664.2:g.29220828T>C	GRCh38
NC_000002.11:g.29443694T>C , CM000664.1:g.29443694T>C	GRCh37
NC_000002.10:g.29297198T>C	NCBI36
NG_009445.1:g.705739A>G , LRG_488:g.705739A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3523A>G MANE Select	ENSP00000373700.3:p.Asn1175Asp
ENST00000431873.6:c.750A>G
ENST00000638605.1:n.400A>G
ENST00000642122.1:c.319A>G	ENSP00000493203.1:p.Asn107Asp
ENST00000389048.7:c.3523A>G	ENSP00000373700.3:p.Asn1175Asp
ENST00000431873.5:c.403A>G	ENSP00000414027.2:p.Asn135Asp
ENST00000618119.4:c.2392A>G	ENSP00000482733.1:p.Asn798Asp
NM_004304.4:c.3523A>G	NP_004295.2:p.Asn1175Asp
NM_001353765.1:c.319A>G	NP_001340694.1:p.Asn107Asp
XM_024452778.1:c.676A>G	XP_024308546.1:p.Asn226Asp
XM_024452779.1:c.319A>G	XP_024308547.1:p.Asn107Asp
NM_004304.5:c.3523A>G MANE Select	NP_004295.2:p.Asn1175Asp
NM_001353765.2:c.319A>G	NP_001340694.1:p.Asn107Asp