Canonical Allele Identifier: CA1593558

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29193606C>T , CM000664.2:g.29193606C>T GRCh38
NC_000002.11:g.29416472C>T , CM000664.1:g.29416472C>T GRCh37
NC_000002.10:g.29269976C>T NCBI36
NG_009445.1:g.732961G>A , LRG_488:g.732961G>A

Transcript Alleles

HGVS Amino-acid Change
NM_004304.5:c.4481G>A (ALK) MANE Select NP_004295.2:p.Gly1494Glu
ENST00000389048.8:c.4481G>A (ALK) MANE Select ENSP00000373700.3:p.Gly1494Glu
NM_001353765.1:c.1277G>A (ALK) NP_001340694.1:p.Gly426Glu
NM_001353765.2:c.1277G>A (ALK) NP_001340694.1:p.Gly426Glu
NM_004304.4:c.4481G>A (ALK) NP_004295.2:p.Gly1494Glu
ENST00000389048.7:c.4481G>A (ALK) ENSP00000373700.3:p.Gly1494Glu
ENST00000431873.5:c.1361G>A (ALK) ENSP00000414027.2:p.Gly454Glu
ENST00000431873.6:c.1708G>A (ALK)
ENST00000618119.4:c.3350G>A (ALK) ENSP00000482733.1:p.Gly1117Glu
ENST00000638605.1:n.1358G>A (ALK)
ENST00000642122.1:c.1277G>A (ALK) ENSP00000493203.1:p.Gly426Glu
ENST00000689605.1:c.1923-3322C>T (CLIP4) ENSP00000508948.1:n.1923-3322C>T
XM_024452778.1:c.1634G>A (ALK) XP_024308546.1:p.Gly545Glu
XM_024452779.1:c.1277G>A (ALK) XP_024308547.1:p.Gly426Glu