Canonical Allele Identifier: CA425619417

Gene: ALK

Linked Data

• dbSNP Id: rs1159752067
• MyVariant Identifiers: chr2:g.29443647C>T (hg19) ; chr2:g.29220781C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220781C>T , CM000664.2:g.29220781C>T	GRCh38
NC_000002.11:g.29443647C>T , CM000664.1:g.29443647C>T	GRCh37
NC_000002.10:g.29297151C>T	NCBI36
NG_009445.1:g.705786G>A , LRG_488:g.705786G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3570G>A MANE Select	ENSP00000373700.3:p.Leu1190=
ENST00000431873.6:c.797G>A
ENST00000638605.1:n.447G>A
ENST00000642122.1:c.366G>A	ENSP00000493203.1:p.Leu122=
ENST00000389048.7:c.3570G>A	ENSP00000373700.3:p.Leu1190=
ENST00000431873.5:c.450G>A	ENSP00000414027.2:p.Leu150=
ENST00000618119.4:c.2439G>A	ENSP00000482733.1:p.Leu813=
NM_004304.4:c.3570G>A	NP_004295.2:p.Leu1190=
NM_001353765.1:c.366G>A	NP_001340694.1:p.Leu122=
XM_024452778.1:c.723G>A	XP_024308546.1:p.Leu241=
XM_024452779.1:c.366G>A	XP_024308547.1:p.Leu122=
NM_004304.5:c.3570G>A MANE Select	NP_004295.2:p.Leu1190=
NM_001353765.2:c.366G>A	NP_001340694.1:p.Leu122=