Canonical Allele Identifier: CA425436030

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29449930G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29227064G>C , CM000664.2:g.29227064G>C	GRCh38
NC_000002.11:g.29449930G>C , CM000664.1:g.29449930G>C	GRCh37
NC_000002.10:g.29303434G>C	NCBI36
NG_009445.1:g.699503C>G , LRG_488:g.699503C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.2925C>G MANE Select	ENSP00000373700.3:p.Gly975=
ENST00000431873.6:c.91C>G
ENST00000389048.7:c.2925C>G	ENSP00000373700.3:p.Gly975=
ENST00000618119.4:c.1794C>G	ENSP00000482733.1:p.Gly598=
NM_004304.4:c.2925C>G	NP_004295.2:p.Gly975=
XM_024452778.1:c.78C>G	XP_024308546.1:p.Gly26=
XR_001738688.2:n.3781C>G
NM_004304.5:c.2925C>G MANE Select	NP_004295.2:p.Gly975=