Canonical Allele Identifier: CA346465863

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29197560T>A , CM000664.2:g.29197560T>A GRCh38
NC_000002.11:g.29420426T>A , CM000664.1:g.29420426T>A GRCh37
NC_000002.10:g.29273930T>A NCBI36
NG_009445.1:g.729007A>T , LRG_488:g.729007A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000689605.1:c.*554T>A (CLIP4) ENSP00000508948.1:n.*554T>A
ENST00000389048.8:c.4055A>T (ALK) MANE Select ENSP00000373700.3:p.Lys1352Met
ENST00000431873.6:c.1282A>T (ALK)
ENST00000638605.1:n.932A>T (ALK)
ENST00000642122.1:c.851A>T (ALK) ENSP00000493203.1:p.Lys284Met
ENST00000389048.7:c.4055A>T (ALK) ENSP00000373700.3:p.Lys1352Met
ENST00000431873.5:c.935A>T (ALK) ENSP00000414027.2:p.Lys312Met
ENST00000618119.4:c.2924A>T (ALK) ENSP00000482733.1:p.Lys975Met
NM_004304.4:c.4055A>T (ALK) NP_004295.2:p.Lys1352Met
NM_001353765.1:c.851A>T (ALK) NP_001340694.1:p.Lys284Met
XM_024452778.1:c.1208A>T (ALK) XP_024308546.1:p.Lys403Met
XM_024452779.1:c.851A>T (ALK) XP_024308547.1:p.Lys284Met
NM_004304.5:c.4055A>T (ALK) MANE Select NP_004295.2:p.Lys1352Met
NM_001353765.2:c.851A>T (ALK) NP_001340694.1:p.Lys284Met