Canonical Allele Identifier: CA346473116

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29443661T>G (hg19) ; chr2:g.29220795T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220795T>G , CM000664.2:g.29220795T>G	GRCh38
NC_000002.11:g.29443661T>G , CM000664.1:g.29443661T>G	GRCh37
NC_000002.10:g.29297165T>G	NCBI36
NG_009445.1:g.705772A>C , LRG_488:g.705772A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.3556A>C MANE Select	ENSP00000373700.3:p.Ser1186Arg
ENST00000431873.6:c.783A>C
ENST00000638605.1:n.433A>C
ENST00000642122.1:c.352A>C	ENSP00000493203.1:p.Ser118Arg
ENST00000389048.7:c.3556A>C	ENSP00000373700.3:p.Ser1186Arg
ENST00000431873.5:c.436A>C	ENSP00000414027.2:p.Ser146Arg
ENST00000618119.4:c.2425A>C	ENSP00000482733.1:p.Ser809Arg
NM_004304.4:c.3556A>C	NP_004295.2:p.Ser1186Arg
NM_001353765.1:c.352A>C	NP_001340694.1:p.Ser118Arg
XM_024452778.1:c.709A>C	XP_024308546.1:p.Ser237Arg
XM_024452779.1:c.352A>C	XP_024308547.1:p.Ser118Arg
NM_004304.5:c.3556A>C MANE Select	NP_004295.2:p.Ser1186Arg
NM_001353765.2:c.352A>C	NP_001340694.1:p.Ser118Arg