Canonical Allele Identifier: CA425619389

Gene: ALK

Linked Data

• dbSNP Id: rs2148166397
• MyVariant Identifiers: chr2:g.29443605G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220739G>A , CM000664.2:g.29220739G>A	GRCh38
NC_000002.11:g.29443605G>A , CM000664.1:g.29443605G>A	GRCh37
NC_000002.10:g.29297109G>A	NCBI36
NG_009445.1:g.705828C>T , LRG_488:g.705828C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3612C>T MANE Select	ENSP00000373700.3:p.Leu1204=
ENST00000431873.6:c.839C>T
ENST00000638605.1:n.489C>T
ENST00000642122.1:c.408C>T	ENSP00000493203.1:p.Leu136=
ENST00000389048.7:c.3612C>T	ENSP00000373700.3:p.Leu1204=
ENST00000431873.5:c.492C>T	ENSP00000414027.2:p.Leu164=
ENST00000618119.4:c.2481C>T	ENSP00000482733.1:p.Leu827=
NM_004304.4:c.3612C>T	NP_004295.2:p.Leu1204=
NM_001353765.1:c.408C>T	NP_001340694.1:p.Leu136=
XM_024452778.1:c.765C>T	XP_024308546.1:p.Leu255=
XM_024452779.1:c.408C>T	XP_024308547.1:p.Leu136=
NM_004304.5:c.3612C>T MANE Select	NP_004295.2:p.Leu1204=
NM_001353765.2:c.408C>T	NP_001340694.1:p.Leu136=