Canonical Allele Identifier: CA425434587

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29445263T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222397T>C , CM000664.2:g.29222397T>C	GRCh38
NC_000002.11:g.29445263T>C , CM000664.1:g.29445263T>C	GRCh37
NC_000002.10:g.29298767T>C	NCBI36
NG_009445.1:g.704170A>G , LRG_488:g.704170A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3462A>G MANE Select	ENSP00000373700.3:p.Glu1154=
ENST00000431873.6:c.689A>G
ENST00000638605.1:n.339A>G
ENST00000642122.1:c.258A>G	ENSP00000493203.1:p.Glu86=
ENST00000389048.7:c.3462A>G	ENSP00000373700.3:p.Glu1154=
ENST00000431873.5:c.342A>G	ENSP00000414027.2:p.Glu114=
ENST00000453137.1:c.156A>G	ENSP00000387488.1:p.Glu52=
ENST00000618119.4:c.2331A>G	ENSP00000482733.1:p.Glu777=
NM_004304.4:c.3462A>G	NP_004295.2:p.Glu1154=
NM_001353765.1:c.258A>G	NP_001340694.1:p.Glu86=
XM_024452778.1:c.615A>G	XP_024308546.1:p.Glu205=
XM_024452779.1:c.258A>G	XP_024308547.1:p.Glu86=
NM_004304.5:c.3462A>G MANE Select	NP_004295.2:p.Glu1154=
NM_001353765.2:c.258A>G	NP_001340694.1:p.Glu86=