Canonical Allele Identifier: CA346463927
Community Standard Title: NM_004304.5(ALK):c.3406T>G (p.Ser1136Ala)
Gene: ALK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29222561A>C , CM000664.2:g.29222561A>C GRCh38
NC_000002.11:g.29445427A>C , CM000664.1:g.29445427A>C GRCh37
NC_000002.10:g.29298931A>C NCBI36
NG_009445.1:g.704006T>G , LRG_488:g.704006T>G

Transcript Alleles

HGVS Amino-acid Change
NM_004304.5:c.3406T>G MANE Select NP_004295.2:p.Ser1136Ala
ENST00000389048.8:c.3406T>G MANE Select ENSP00000373700.3:p.Ser1136Ala
NM_001353765.1:c.202T>G NP_001340694.1:p.Ser68Ala
NM_001353765.2:c.202T>G NP_001340694.1:p.Ser68Ala
NM_004304.4:c.3406T>G NP_004295.2:p.Ser1136Ala
ENST00000389048.7:c.3406T>G ENSP00000373700.3:p.Ser1136Ala
ENST00000431873.5:c.286T>G ENSP00000414027.2:p.Ser96Ala
ENST00000431873.6:c.633T>G
ENST00000453137.1:c.100T>G ENSP00000387488.1:p.Ser34Ala
ENST00000618119.4:c.2275T>G ENSP00000482733.1:p.Ser759Ala
ENST00000638605.1:n.283T>G
ENST00000642122.1:c.202T>G ENSP00000493203.1:p.Ser68Ala
XM_024452778.1:c.559T>G XP_024308546.1:p.Ser187Ala
XM_024452779.1:c.202T>G XP_024308547.1:p.Ser68Ala