Canonical Allele Identifier: CA346461245
Community Standard Title: NM_004304.5(ALK):c.4493A>G (p.Lys1498Arg)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29193594T>C , CM000664.2:g.29193594T>C GRCh38
NC_000002.11:g.29416460T>C , CM000664.1:g.29416460T>C GRCh37
NC_000002.10:g.29269964T>C NCBI36
NG_009445.1:g.732973A>G , LRG_488:g.732973A>G

Transcript Alleles

HGVS Amino-acid Change
NM_004304.5:c.4493A>G (ALK) MANE Select NP_004295.2:p.Lys1498Arg
ENST00000389048.8:c.4493A>G (ALK) MANE Select ENSP00000373700.3:p.Lys1498Arg
NM_001353765.1:c.1289A>G (ALK) NP_001340694.1:p.Lys430Arg
NM_001353765.2:c.1289A>G (ALK) NP_001340694.1:p.Lys430Arg
NM_004304.4:c.4493A>G (ALK) NP_004295.2:p.Lys1498Arg
ENST00000389048.7:c.4493A>G (ALK) ENSP00000373700.3:p.Lys1498Arg
ENST00000431873.5:c.1373A>G (ALK) ENSP00000414027.2:p.Lys458Arg
ENST00000431873.6:c.1720A>G (ALK)
ENST00000618119.4:c.3362A>G (ALK) ENSP00000482733.1:p.Lys1121Arg
ENST00000638605.1:n.1370A>G (ALK)
ENST00000642122.1:c.1289A>G (ALK) ENSP00000493203.1:p.Lys430Arg
ENST00000689605.1:c.1923-3334T>C (CLIP4) ENSP00000508948.1:n.1923-3334T>C
XM_024452778.1:c.1646A>G (ALK) XP_024308546.1:p.Lys549Arg
XM_024452779.1:c.1289A>G (ALK) XP_024308547.1:p.Lys430Arg