Canonical Allele Identifier: CA425434559

Gene: ALK

Linked Data

• dbSNP Id: rs2148168572
• MyVariant Identifiers: chr2:g.29445218C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222352C>G , CM000664.2:g.29222352C>G	GRCh38
NC_000002.11:g.29445218C>G , CM000664.1:g.29445218C>G	GRCh37
NC_000002.10:g.29298722C>G	NCBI36
NG_009445.1:g.704215G>C , LRG_488:g.704215G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3507G>C MANE Select	ENSP00000373700.3:p.Leu1169=
ENST00000431873.6:c.734G>C
ENST00000638605.1:n.384G>C
ENST00000642122.1:c.303G>C	ENSP00000493203.1:p.Leu101=
ENST00000389048.7:c.3507G>C	ENSP00000373700.3:p.Leu1169=
ENST00000431873.5:c.387G>C	ENSP00000414027.2:p.Leu129=
ENST00000453137.1:c.201G>C	ENSP00000387488.1:p.Leu67=
ENST00000618119.4:c.2376G>C	ENSP00000482733.1:p.Leu792=
NM_004304.4:c.3507G>C	NP_004295.2:p.Leu1169=
NM_001353765.1:c.303G>C	NP_001340694.1:p.Leu101=
XM_024452778.1:c.660G>C	XP_024308546.1:p.Leu220=
XM_024452779.1:c.303G>C	XP_024308547.1:p.Leu101=
NM_004304.5:c.3507G>C MANE Select	NP_004295.2:p.Leu1169=
NM_001353765.2:c.303G>C	NP_001340694.1:p.Leu101=