Canonical Allele Identifier: CA346462952

Gene: ALK

Linked Data

• dbSNP Id: rs2148168593
• COSMIC: COSM50288
• MyVariant Identifiers: chr2:g.29445223C>G (hg19) ; chr2:g.29222357C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222357C>G , CM000664.2:g.29222357C>G	GRCh38
NC_000002.11:g.29445223C>G , CM000664.1:g.29445223C>G	GRCh37
NC_000002.10:g.29298727C>G	NCBI36
NG_009445.1:g.704210G>C , LRG_488:g.704210G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3502G>C MANE Select	ENSP00000373700.3:p.Ala1168Pro
ENST00000431873.6:c.729G>C
ENST00000638605.1:n.379G>C
ENST00000642122.1:c.298G>C	ENSP00000493203.1:p.Ala100Pro
ENST00000389048.7:c.3502G>C	ENSP00000373700.3:p.Ala1168Pro
ENST00000431873.5:c.382G>C	ENSP00000414027.2:p.Ala128Pro
ENST00000453137.1:c.196G>C	ENSP00000387488.1:p.Ala66Pro
ENST00000618119.4:c.2371G>C	ENSP00000482733.1:p.Ala791Pro
NM_004304.4:c.3502G>C	NP_004295.2:p.Ala1168Pro
NM_001353765.1:c.298G>C	NP_001340694.1:p.Ala100Pro
XM_024452778.1:c.655G>C	XP_024308546.1:p.Ala219Pro
XM_024452779.1:c.298G>C	XP_024308547.1:p.Ala100Pro
NM_004304.5:c.3502G>C MANE Select	NP_004295.2:p.Ala1168Pro
NM_001353765.2:c.298G>C	NP_001340694.1:p.Ala100Pro