Canonical Allele Identifier: CA425436069

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29551310G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29328444G>C , CM000664.2:g.29328444G>C	GRCh38
NC_000002.11:g.29551310G>C , CM000664.1:g.29551310G>C	GRCh37
NC_000002.10:g.29404814G>C	NCBI36
NG_009445.1:g.598123C>G , LRG_488:g.598123C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.1320C>G MANE Select	ENSP00000373700.3:p.Ser440=
ENST00000389048.7:c.1320C>G	ENSP00000373700.3:p.Ser440=
ENST00000618119.4:c.189C>G	ENSP00000482733.1:p.Ser63=
NM_004304.4:c.1320C>G	NP_004295.2:p.Ser440=
XR_939920.1:n.752G>C
XR_939921.1:n.680+5916G>C
XR_001738688.2:n.2250C>G
XR_939920.2:n.642G>C
XR_939921.2:n.576+5916G>C
NM_004304.5:c.1320C>G MANE Select	NP_004295.2:p.Ser440=