Canonical Allele Identifier: CA346463059

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29445236A>C (hg19) ; chr2:g.29222370A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222370A>C , CM000664.2:g.29222370A>C	GRCh38
NC_000002.11:g.29445236A>C , CM000664.1:g.29445236A>C	GRCh37
NC_000002.10:g.29298740A>C	NCBI36
NG_009445.1:g.704197T>G , LRG_488:g.704197T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3489T>G MANE Select	ENSP00000373700.3:p.Asp1163Glu
ENST00000431873.6:c.716T>G
ENST00000638605.1:n.366T>G
ENST00000642122.1:c.285T>G	ENSP00000493203.1:p.Asp95Glu
ENST00000389048.7:c.3489T>G	ENSP00000373700.3:p.Asp1163Glu
ENST00000431873.5:c.369T>G	ENSP00000414027.2:p.Asp123Glu
ENST00000453137.1:c.183T>G	ENSP00000387488.1:p.Asp61Glu
ENST00000618119.4:c.2358T>G	ENSP00000482733.1:p.Asp786Glu
NM_004304.4:c.3489T>G	NP_004295.2:p.Asp1163Glu
NM_001353765.1:c.285T>G	NP_001340694.1:p.Asp95Glu
XM_024452778.1:c.642T>G	XP_024308546.1:p.Asp214Glu
XM_024452779.1:c.285T>G	XP_024308547.1:p.Asp95Glu
NM_004304.5:c.3489T>G MANE Select	NP_004295.2:p.Asp1163Glu
NM_001353765.2:c.285T>G	NP_001340694.1:p.Asp95Glu