Canonical Allele Identifier: CA425434570

Gene: ALK

Linked Data

• dbSNP Id: rs1669826137
• MyVariant Identifiers: chr2:g.29445236A>G (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3489T>C MANE Select	ENSP00000373700.3:p.Asp1163=
ENST00000431873.6:c.716T>C
ENST00000638605.1:n.366T>C
ENST00000642122.1:c.285T>C	ENSP00000493203.1:p.Asp95=
ENST00000389048.7:c.3489T>C	ENSP00000373700.3:p.Asp1163=
ENST00000431873.5:c.369T>C	ENSP00000414027.2:p.Asp123=
ENST00000453137.1:c.183T>C	ENSP00000387488.1:p.Asp61=
ENST00000618119.4:c.2358T>C	ENSP00000482733.1:p.Asp786=
NM_004304.4:c.3489T>C	NP_004295.2:p.Asp1163=
NM_001353765.1:c.285T>C	NP_001340694.1:p.Asp95=
XM_024452778.1:c.642T>C	XP_024308546.1:p.Asp214=
XM_024452779.1:c.285T>C	XP_024308547.1:p.Asp95=
NM_004304.5:c.3489T>C MANE Select	NP_004295.2:p.Asp1163=
NM_001353765.2:c.285T>C	NP_001340694.1:p.Asp95=