Canonical Allele Identifier: CA346467631

Gene: ALK

Linked Data

• dbSNP Id: rs1553395221
• MyVariant Identifiers: chr2:g.29449838C>G (hg19) ; chr2:g.29226972C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29226972C>G , CM000664.2:g.29226972C>G	GRCh38
NC_000002.11:g.29449838C>G , CM000664.1:g.29449838C>G	GRCh37
NC_000002.10:g.29303342C>G	NCBI36
NG_009445.1:g.699595G>C , LRG_488:g.699595G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3017G>C MANE Select	ENSP00000373700.3:p.Cys1006Ser
ENST00000431873.6:c.183G>C
ENST00000389048.7:c.3017G>C	ENSP00000373700.3:p.Cys1006Ser
ENST00000618119.4:c.1886G>C	ENSP00000482733.1:p.Cys629Ser
NM_004304.4:c.3017G>C	NP_004295.2:p.Cys1006Ser
XM_024452778.1:c.170G>C	XP_024308546.1:p.Cys57Ser
XR_001738688.2:n.3873G>C
NM_004304.5:c.3017G>C MANE Select	NP_004295.2:p.Cys1006Ser