Canonical Allele Identifier: CA346473109

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29443658G>C (hg19) ; chr2:g.29220792G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220792G>C , CM000664.2:g.29220792G>C	GRCh38
NC_000002.11:g.29443658G>C , CM000664.1:g.29443658G>C	GRCh37
NC_000002.10:g.29297162G>C	NCBI36
NG_009445.1:g.705775C>G , LRG_488:g.705775C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.3559C>G MANE Select	ENSP00000373700.3:p.Leu1187Val
ENST00000431873.6:c.786C>G
ENST00000638605.1:n.436C>G
ENST00000642122.1:c.355C>G	ENSP00000493203.1:p.Leu119Val
ENST00000389048.7:c.3559C>G	ENSP00000373700.3:p.Leu1187Val
ENST00000431873.5:c.439C>G	ENSP00000414027.2:p.Leu147Val
ENST00000618119.4:c.2428C>G	ENSP00000482733.1:p.Leu810Val
NM_004304.4:c.3559C>G	NP_004295.2:p.Leu1187Val
NM_001353765.1:c.355C>G	NP_001340694.1:p.Leu119Val
XM_024452778.1:c.712C>G	XP_024308546.1:p.Leu238Val
XM_024452779.1:c.355C>G	XP_024308547.1:p.Leu119Val
NM_004304.5:c.3559C>G MANE Select	NP_004295.2:p.Leu1187Val
NM_001353765.2:c.355C>G	NP_001340694.1:p.Leu119Val