Canonical Allele Identifier: CA346473193

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29443699T>A (hg19) ; chr2:g.29220833T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220833T>A , CM000664.2:g.29220833T>A	GRCh38
NC_000002.11:g.29443699T>A , CM000664.1:g.29443699T>A	GRCh37
NC_000002.10:g.29297203T>A	NCBI36
NG_009445.1:g.705734A>T , LRG_488:g.705734A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3518A>T MANE Select	ENSP00000373700.3:p.Lys1173Ile
ENST00000431873.6:c.745A>T
ENST00000638605.1:n.395A>T
ENST00000642122.1:c.314A>T	ENSP00000493203.1:p.Lys105Ile
ENST00000389048.7:c.3518A>T	ENSP00000373700.3:p.Lys1173Ile
ENST00000431873.5:c.398A>T	ENSP00000414027.2:p.Lys133Ile
ENST00000618119.4:c.2387A>T	ENSP00000482733.1:p.Lys796Ile
NM_004304.4:c.3518A>T	NP_004295.2:p.Lys1173Ile
NM_001353765.1:c.314A>T	NP_001340694.1:p.Lys105Ile
XM_024452778.1:c.671A>T	XP_024308546.1:p.Lys224Ile
XM_024452779.1:c.314A>T	XP_024308547.1:p.Lys105Ile
NM_004304.5:c.3518A>T MANE Select	NP_004295.2:p.Lys1173Ile
NM_001353765.2:c.314A>T	NP_001340694.1:p.Lys105Ile