Canonical Allele Identifier: CA376401374

Gene: WAC

Linked Data

• ClinVar Variation Id: 445335
• ClinVar RCV Id: RCV000513980
• dbSNP Id: rs1554787110
• gnomAD v4: 10-28589791-A-G
• MyVariant Identifiers: chr10:g.28878720A>G (hg19) ; chr10:g.28589791A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.28589791A>G , CM000672.2:g.28589791A>G	GRCh38
NC_000010.10:g.28878720A>G , CM000672.1:g.28878720A>G	GRCh37
NC_000010.9:g.28918726A>G	NCBI36
NG_046603.1:g.62204A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700325.1:c.425A>G	ENSP00000514952.1:p.Tyr142Cys
ENST00000706612.1:c.427A>G	ENSP00000516469.1:p.Thr143Ala
ENST00000354911.9:c.437A>G MANE Select	ENSP00000346986.4:p.Tyr146Cys
ENST00000414108.6:c.302A>G	ENSP00000415645.2:p.Tyr101Cys
ENST00000420266.6:c.*351A>G	ENSP00000404758.2:n.*351A>G
ENST00000428935.6:c.302A>G	ENSP00000399706.3:p.Tyr101Cys
ENST00000442148.6:c.302A>G	ENSP00000400848.2:p.Tyr101Cys
ENST00000628285.3:c.295A>G	ENSP00000486994.2:p.Thr99Ala
ENST00000651441.1:c.302A>G	ENSP00000498450.1:p.Tyr101Cys
ENST00000651598.1:c.302A>G	ENSP00000498480.1:p.Tyr101Cys
ENST00000651885.1:c.455A>G	ENSP00000498678.1:p.Tyr152Cys
ENST00000679398.1:c.302A>G	ENSP00000506624.1:p.Tyr101Cys
ENST00000679428.1:c.302A>G	ENSP00000506445.1:p.Tyr101Cys
ENST00000679570.1:c.*432A>G	ENSP00000506705.1:n.*432A>G
ENST00000680735.1:c.310A>G	ENSP00000505513.1:p.Thr104Ala
ENST00000681112.1:c.*290A>G	ENSP00000505444.1:n.*290A>G
ENST00000345541.6:n.235A>G
ENST00000347934.8:c.437A>G	ENSP00000311106.4:p.Tyr146Cys
ENST00000354911.8:c.437A>G	ENSP00000346986.4:p.Tyr146Cys
ENST00000375646.5:c.302A>G	ENSP00000364797.1:p.Tyr101Cys
ENST00000375664.8:c.302A>G	ENSP00000364816.3:p.Tyr101Cys
ENST00000414108.5:c.302A>G	ENSP00000415645.1:p.Tyr101Cys
ENST00000420266.5:c.302A>G	ENSP00000404758.1:p.Tyr101Cys
ENST00000424454.5:c.*445A>G	ENSP00000404125.2:n.*445A>G
ENST00000428935.5:c.310A>G	ENSP00000399706.2:p.Thr104Ala
ENST00000439676.5:c.302A>G	ENSP00000415727.1:p.Tyr101Cys
ENST00000442148.5:c.302A>G	ENSP00000400848.1:p.Tyr101Cys
ENST00000472862.1:n.1055A>G
ENST00000628285.2:c.310A>G	ENSP00000486994.1:p.Thr104Ala
NM_016628.4:c.437A>G	NP_057712.2:p.Tyr146Cys
NM_100264.2:c.302A>G	NP_567822.1:p.Tyr101Cys
NM_100486.3:c.437A>G	NP_567823.1:p.Tyr146Cys
XM_005252454.2:c.455A>G	XP_005252511.1:p.Tyr152Cys
XM_011519491.1:c.302A>G	XP_011517793.1:p.Tyr101Cys
XR_930491.1:n.357A>G
XM_017016315.2:c.302A>G	XP_016871804.1:p.Tyr101Cys
XM_017016317.2:c.302A>G	XP_016871806.1:p.Tyr101Cys
XM_017016318.2:c.302A>G	XP_016871807.1:p.Tyr101Cys
XM_024448036.1:c.302A>G	XP_024303804.1:p.Tyr101Cys
XR_001747110.1:n.392A>G
XR_930491.2:n.357A>G
NM_016628.5:c.437A>G MANE Select	NP_057712.2:p.Tyr146Cys
NM_100264.3:c.302A>G	NP_567822.1:p.Tyr101Cys
NM_100486.4:c.437A>G	NP_567823.1:p.Tyr146Cys