Canonical Allele Identifier: CA425434579

Gene: ALK

Linked Data

• dbSNP Id: rs2148168665
• MyVariant Identifiers: chr2:g.29445248C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222382C>T , CM000664.2:g.29222382C>T	GRCh38
NC_000002.11:g.29445248C>T , CM000664.1:g.29445248C>T	GRCh37
NC_000002.10:g.29298752C>T	NCBI36
NG_009445.1:g.704185G>A , LRG_488:g.704185G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3477G>A MANE Select	ENSP00000373700.3:p.Gln1159=
ENST00000431873.6:c.704G>A
ENST00000638605.1:n.354G>A
ENST00000642122.1:c.273G>A	ENSP00000493203.1:p.Gln91=
ENST00000389048.7:c.3477G>A	ENSP00000373700.3:p.Gln1159=
ENST00000431873.5:c.357G>A	ENSP00000414027.2:p.Gln119=
ENST00000453137.1:c.171G>A	ENSP00000387488.1:p.Gln57=
ENST00000618119.4:c.2346G>A	ENSP00000482733.1:p.Gln782=
NM_004304.4:c.3477G>A	NP_004295.2:p.Gln1159=
NM_001353765.1:c.273G>A	NP_001340694.1:p.Gln91=
XM_024452778.1:c.630G>A	XP_024308546.1:p.Gln210=
XM_024452779.1:c.273G>A	XP_024308547.1:p.Gln91=
NM_004304.5:c.3477G>A MANE Select	NP_004295.2:p.Gln1159=
NM_001353765.2:c.273G>A	NP_001340694.1:p.Gln91=