Canonical Allele Identifier: CA425434563

Gene: ALK

Linked Data

• ClinVar Variation Id: 1732097
• ClinVar RCV Id: RCV002459167 ; RCV003102386
• dbSNP Id: rs1669825838
• MyVariant Identifiers: chr2:g.29445221G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222355G>C , CM000664.2:g.29222355G>C	GRCh38
NC_000002.11:g.29445221G>C , CM000664.1:g.29445221G>C	GRCh37
NC_000002.10:g.29298725G>C	NCBI36
NG_009445.1:g.704212C>G , LRG_488:g.704212C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3504C>G MANE Select	ENSP00000373700.3:p.Ala1168=
ENST00000431873.6:c.731C>G
ENST00000638605.1:n.381C>G
ENST00000642122.1:c.300C>G	ENSP00000493203.1:p.Ala100=
ENST00000389048.7:c.3504C>G	ENSP00000373700.3:p.Ala1168=
ENST00000431873.5:c.384C>G	ENSP00000414027.2:p.Ala128=
ENST00000453137.1:c.198C>G	ENSP00000387488.1:p.Ala66=
ENST00000618119.4:c.2373C>G	ENSP00000482733.1:p.Ala791=
NM_004304.4:c.3504C>G	NP_004295.2:p.Ala1168=
NM_001353765.1:c.300C>G	NP_001340694.1:p.Ala100=
XM_024452778.1:c.657C>G	XP_024308546.1:p.Ala219=
XM_024452779.1:c.300C>G	XP_024308547.1:p.Ala100=
NM_004304.5:c.3504C>G MANE Select	NP_004295.2:p.Ala1168=
NM_001353765.2:c.300C>G	NP_001340694.1:p.Ala100=