Canonical Allele Identifier: CA346462949

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29445223C>A (hg19) ; chr2:g.29222357C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222357C>A , CM000664.2:g.29222357C>A	GRCh38
NC_000002.11:g.29445223C>A , CM000664.1:g.29445223C>A	GRCh37
NC_000002.10:g.29298727C>A	NCBI36
NG_009445.1:g.704210G>T , LRG_488:g.704210G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3502G>T MANE Select	ENSP00000373700.3:p.Ala1168Ser
ENST00000431873.6:c.729G>T
ENST00000638605.1:n.379G>T
ENST00000642122.1:c.298G>T	ENSP00000493203.1:p.Ala100Ser
ENST00000389048.7:c.3502G>T	ENSP00000373700.3:p.Ala1168Ser
ENST00000431873.5:c.382G>T	ENSP00000414027.2:p.Ala128Ser
ENST00000453137.1:c.196G>T	ENSP00000387488.1:p.Ala66Ser
ENST00000618119.4:c.2371G>T	ENSP00000482733.1:p.Ala791Ser
NM_004304.4:c.3502G>T	NP_004295.2:p.Ala1168Ser
NM_001353765.1:c.298G>T	NP_001340694.1:p.Ala100Ser
XM_024452778.1:c.655G>T	XP_024308546.1:p.Ala219Ser
XM_024452779.1:c.298G>T	XP_024308547.1:p.Ala100Ser
NM_004304.5:c.3502G>T MANE Select	NP_004295.2:p.Ala1168Ser
NM_001353765.2:c.298G>T	NP_001340694.1:p.Ala100Ser