Canonical Allele Identifier: CA346463191

Gene: ALK

Linked Data

• dbSNP Id: rs1228794467
• MyVariant Identifiers: chr2:g.29445251T>G (hg19) ; chr2:g.29222385T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222385T>G , CM000664.2:g.29222385T>G	GRCh38
NC_000002.11:g.29445251T>G , CM000664.1:g.29445251T>G	GRCh37
NC_000002.10:g.29298755T>G	NCBI36
NG_009445.1:g.704182A>C , LRG_488:g.704182A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3474A>C MANE Select	ENSP00000373700.3:p.Glu1158Asp
ENST00000431873.6:c.701A>C
ENST00000638605.1:n.351A>C
ENST00000642122.1:c.270A>C	ENSP00000493203.1:p.Glu90Asp
ENST00000389048.7:c.3474A>C	ENSP00000373700.3:p.Glu1158Asp
ENST00000431873.5:c.354A>C	ENSP00000414027.2:p.Glu118Asp
ENST00000453137.1:c.168A>C	ENSP00000387488.1:p.Glu56Asp
ENST00000618119.4:c.2343A>C	ENSP00000482733.1:p.Glu781Asp
NM_004304.4:c.3474A>C	NP_004295.2:p.Glu1158Asp
NM_001353765.1:c.270A>C	NP_001340694.1:p.Glu90Asp
XM_024452778.1:c.627A>C	XP_024308546.1:p.Glu209Asp
XM_024452779.1:c.270A>C	XP_024308547.1:p.Glu90Asp
NM_004304.5:c.3474A>C MANE Select	NP_004295.2:p.Glu1158Asp
NM_001353765.2:c.270A>C	NP_001340694.1:p.Glu90Asp