Canonical Allele Identifier: CA425619391

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29443611T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220745T>A , CM000664.2:g.29220745T>A	GRCh38
NC_000002.11:g.29443611T>A , CM000664.1:g.29443611T>A	GRCh37
NC_000002.10:g.29297115T>A	NCBI36
NG_009445.1:g.705822A>T , LRG_488:g.705822A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3606A>T MANE Select	ENSP00000373700.3:p.Gly1202=
ENST00000431873.6:c.833A>T
ENST00000638605.1:n.483A>T
ENST00000642122.1:c.402A>T	ENSP00000493203.1:p.Gly134=
ENST00000389048.7:c.3606A>T	ENSP00000373700.3:p.Gly1202=
ENST00000431873.5:c.486A>T	ENSP00000414027.2:p.Gly162=
ENST00000618119.4:c.2475A>T	ENSP00000482733.1:p.Gly825=
NM_004304.4:c.3606A>T	NP_004295.2:p.Gly1202=
NM_001353765.1:c.402A>T	NP_001340694.1:p.Gly134=
XM_024452778.1:c.759A>T	XP_024308546.1:p.Gly253=
XM_024452779.1:c.402A>T	XP_024308547.1:p.Gly134=
NM_004304.5:c.3606A>T MANE Select	NP_004295.2:p.Gly1202=
NM_001353765.2:c.402A>T	NP_001340694.1:p.Gly134=