Canonical Allele Identifier: CA16606012
Gene: WAC HGNC NCBI

Linked Data

ClinVar Variation Id: 392418
ClinVar RCV Id: RCV000444436
dbSNP Id: rs1057524482
MyVariant Identifiers: chr10:g.28900760C>G (hg19) chr10:g.28611831C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.28611831C>G , CM000672.2:g.28611831C>G GRCh38
NC_000010.10:g.28900760C>G , CM000672.1:g.28900760C>G GRCh37
NC_000010.9:g.28940766C>G NCBI36
NG_046603.1:g.84244C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000495268.3:c.1438C>G ENSP00000514964.1:n.1438C>G
ENST00000700325.1:c.1334C>G ENSP00000514952.1:p.Ser445Ter
ENST00000706612.1:c.1334C>G ENSP00000516469.1:p.Ser445Ter
ENST00000354911.9:c.1346C>G MANE Select ENSP00000346986.4:p.Ser449Ter
ENST00000414108.6:c.1211C>G ENSP00000415645.2:p.Ser404Ter
ENST00000420266.6:c.*1260C>G ENSP00000404758.2:n.*1260C>G
ENST00000442148.6:c.1211C>G ENSP00000400848.2:p.Ser404Ter
ENST00000628285.3:c.*772C>G ENSP00000486994.2:n.*772C>G
ENST00000679398.1:c.1211C>G ENSP00000506624.1:p.Ser404Ter
ENST00000679428.1:c.1211C>G ENSP00000506445.1:p.Ser404Ter
ENST00000679570.1:c.*1341C>G ENSP00000506705.1:n.*1341C>G
ENST00000680735.1:c.1217C>G ENSP00000505513.1:p.Ser406Ter
ENST00000681112.1:c.*1199C>G ENSP00000505444.1:n.*1199C>G
ENST00000345541.6:n.2087C>G
ENST00000347934.8:c.1037C>G ENSP00000311106.4:p.Ser346Ter
ENST00000354911.8:c.1346C>G ENSP00000346986.4:p.Ser449Ter
ENST00000375646.5:c.890C>G ENSP00000364797.1:p.Ser297Ter
ENST00000375664.8:c.1211C>G ENSP00000364816.3:p.Ser404Ter
ENST00000439676.5:c.*127C>G ENSP00000415727.1:n.*127C>G
ENST00000628285.2:c.*999C>G ENSP00000486994.1:n.*999C>G
NM_016628.4:c.1346C>G NP_057712.2:p.Ser449Ter
NM_100264.2:c.1211C>G NP_567822.1:p.Ser404Ter
NM_100486.3:c.1037C>G NP_567823.1:p.Ser346Ter
XM_005252454.2:c.1364C>G XP_005252511.1:p.Ser455Ter
XM_011519491.1:c.1211C>G XP_011517793.1:p.Ser404Ter
XR_930491.1:n.1493C>G
XM_017016315.2:c.1211C>G XP_016871804.1:p.Ser404Ter
XM_017016317.2:c.902C>G XP_016871806.1:p.Ser301Ter
XM_017016318.2:c.902C>G XP_016871807.1:p.Ser301Ter
XM_024448036.1:c.1211C>G XP_024303804.1:p.Ser404Ter
XR_001747110.1:n.1528C>G
XR_930491.2:n.1493C>G
NM_016628.5:c.1346C>G MANE Select NP_057712.2:p.Ser449Ter
NM_100264.3:c.1211C>G NP_567822.1:p.Ser404Ter
NM_100486.4:c.1037C>G NP_567823.1:p.Ser346Ter
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