Canonical Allele Identifier: CA346462929

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29445220G>T (hg19) ; chr2:g.29222354G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222354G>T , CM000664.2:g.29222354G>T	GRCh38
NC_000002.11:g.29445220G>T , CM000664.1:g.29445220G>T	GRCh37
NC_000002.10:g.29298724G>T	NCBI36
NG_009445.1:g.704213C>A , LRG_488:g.704213C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3505C>A MANE Select	ENSP00000373700.3:p.Leu1169Met
ENST00000431873.6:c.732C>A
ENST00000638605.1:n.382C>A
ENST00000642122.1:c.301C>A	ENSP00000493203.1:p.Leu101Met
ENST00000389048.7:c.3505C>A	ENSP00000373700.3:p.Leu1169Met
ENST00000431873.5:c.385C>A	ENSP00000414027.2:p.Leu129Met
ENST00000453137.1:c.199C>A	ENSP00000387488.1:p.Leu67Met
ENST00000618119.4:c.2374C>A	ENSP00000482733.1:p.Leu792Met
NM_004304.4:c.3505C>A	NP_004295.2:p.Leu1169Met
NM_001353765.1:c.301C>A	NP_001340694.1:p.Leu101Met
XM_024452778.1:c.658C>A	XP_024308546.1:p.Leu220Met
XM_024452779.1:c.301C>A	XP_024308547.1:p.Leu101Met
NM_004304.5:c.3505C>A MANE Select	NP_004295.2:p.Leu1169Met
NM_001353765.2:c.301C>A	NP_001340694.1:p.Leu101Met