Canonical Allele Identifier: CA425434567

Gene: ALK

Linked Data

• dbSNP Id: rs764123976
• MyVariant Identifiers: chr2:g.29445230G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222364G>C , CM000664.2:g.29222364G>C	GRCh38
NC_000002.11:g.29445230G>C , CM000664.1:g.29445230G>C	GRCh37
NC_000002.10:g.29298734G>C	NCBI36
NG_009445.1:g.704203C>G , LRG_488:g.704203C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3495C>G MANE Select	ENSP00000373700.3:p.Leu1165=
ENST00000431873.6:c.722C>G
ENST00000638605.1:n.372C>G
ENST00000642122.1:c.291C>G	ENSP00000493203.1:p.Leu97=
ENST00000389048.7:c.3495C>G	ENSP00000373700.3:p.Leu1165=
ENST00000431873.5:c.375C>G	ENSP00000414027.2:p.Leu125=
ENST00000453137.1:c.189C>G	ENSP00000387488.1:p.Leu63=
ENST00000618119.4:c.2364C>G	ENSP00000482733.1:p.Leu788=
NM_004304.4:c.3495C>G	NP_004295.2:p.Leu1165=
NM_001353765.1:c.291C>G	NP_001340694.1:p.Leu97=
XM_024452778.1:c.648C>G	XP_024308546.1:p.Leu216=
XM_024452779.1:c.291C>G	XP_024308547.1:p.Leu97=
NM_004304.5:c.3495C>G MANE Select	NP_004295.2:p.Leu1165=
NM_001353765.2:c.291C>G	NP_001340694.1:p.Leu97=