Canonical Allele Identifier: CA346469570

Gene: ALK

Linked Data

• dbSNP Id: rs113994087
• MyVariant Identifiers: chr2:g.29432664C>G (hg19) ; chr2:g.29209798C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29209798C>G , CM000664.2:g.29209798C>G	GRCh38
NC_000002.11:g.29432664C>G , CM000664.1:g.29432664C>G	GRCh37
NC_000002.10:g.29286168C>G	NCBI36
NG_009445.1:g.716769G>C , LRG_488:g.716769G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.3824G>C MANE Select	ENSP00000373700.3:p.Arg1275Pro
ENST00000431873.6:c.1051G>C
ENST00000638605.1:n.701G>C
ENST00000642122.1:c.620G>C	ENSP00000493203.1:p.Arg207Pro
ENST00000389048.7:c.3824G>C	ENSP00000373700.3:p.Arg1275Pro
ENST00000431873.5:c.704G>C	ENSP00000414027.2:p.Arg235Pro
ENST00000618119.4:c.2693G>C	ENSP00000482733.1:p.Arg898Pro
NM_004304.4:c.3824G>C	NP_004295.2:p.Arg1275Pro
NM_001353765.1:c.620G>C	NP_001340694.1:p.Arg207Pro
XM_024452778.1:c.977G>C	XP_024308546.1:p.Arg326Pro
XM_024452779.1:c.620G>C	XP_024308547.1:p.Arg207Pro
NM_004304.5:c.3824G>C MANE Select	NP_004295.2:p.Arg1275Pro
NM_001353765.2:c.620G>C	NP_001340694.1:p.Arg207Pro