Canonical Allele Identifier: CA346473197

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29443700T>C (hg19) ; chr2:g.29220834T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220834T>C , CM000664.2:g.29220834T>C	GRCh38
NC_000002.11:g.29443700T>C , CM000664.1:g.29443700T>C	GRCh37
NC_000002.10:g.29297204T>C	NCBI36
NG_009445.1:g.705733A>G , LRG_488:g.705733A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3517A>G MANE Select	ENSP00000373700.3:p.Lys1173Glu
ENST00000431873.6:c.744A>G
ENST00000638605.1:n.394A>G
ENST00000642122.1:c.313A>G	ENSP00000493203.1:p.Lys105Glu
ENST00000389048.7:c.3517A>G	ENSP00000373700.3:p.Lys1173Glu
ENST00000431873.5:c.397A>G	ENSP00000414027.2:p.Lys133Glu
ENST00000618119.4:c.2386A>G	ENSP00000482733.1:p.Lys796Glu
NM_004304.4:c.3517A>G	NP_004295.2:p.Lys1173Glu
NM_001353765.1:c.313A>G	NP_001340694.1:p.Lys105Glu
XM_024452778.1:c.670A>G	XP_024308546.1:p.Lys224Glu
XM_024452779.1:c.313A>G	XP_024308547.1:p.Lys105Glu
NM_004304.5:c.3517A>G MANE Select	NP_004295.2:p.Lys1173Glu
NM_001353765.2:c.313A>G	NP_001340694.1:p.Lys105Glu