Canonical Allele Identifier: CA13217817

Gene: WAC

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.28567890G>A , CM000672.2:g.28567890G>A	GRCh38
NC_000010.10:g.28856819G>A , CM000672.1:g.28856819G>A	GRCh37
NC_000010.9:g.28896825G>A	NCBI36
NG_046603.1:g.40303G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700325.1:c.263-15509G>A	ENSP00000514952.1:n.263-15509G>A
ENST00000706612.1:c.265-15509G>A	ENSP00000516469.1:n.265-15509G>A
ENST00000354911.9:c.275-15509G>A MANE Select	ENSP00000346986.4:n.275-15509G>A
ENST00000414108.6:c.140-15509G>A	ENSP00000415645.2:n.140-15509G>A
ENST00000420266.6:c.*189-15509G>A	ENSP00000404758.2:n.*189-15509G>A
ENST00000428935.6:c.140-15509G>A	ENSP00000399706.3:n.140-15509G>A
ENST00000442148.6:c.140-15509G>A	ENSP00000400848.2:n.140-15509G>A
ENST00000628285.3:c.140-15516G>A	ENSP00000486994.2:n.140-15516G>A
ENST00000651441.1:c.140-15509G>A	ENSP00000498450.1:n.140-15509G>A
ENST00000651598.1:c.140-15509G>A	ENSP00000498480.1:n.140-15509G>A
ENST00000651885.1:c.293-15509G>A	ENSP00000498678.1:n.293-15509G>A
ENST00000679398.1:c.140-15509G>A	ENSP00000506624.1:n.140-15509G>A
ENST00000679428.1:c.140-15509G>A	ENSP00000506445.1:n.140-15509G>A
ENST00000679570.1:c.*270-15509G>A	ENSP00000506705.1:n.*270-15509G>A
ENST00000680735.1:c.148-15509G>A	ENSP00000505513.1:n.148-15509G>A
ENST00000681112.1:c.*128-15509G>A	ENSP00000505444.1:n.*128-15509G>A
ENST00000345541.6:n.73-15509G>A
ENST00000347934.8:c.275-15509G>A	ENSP00000311106.4:n.275-15509G>A
ENST00000354911.8:c.275-15509G>A	ENSP00000346986.4:n.275-15509G>A
ENST00000375646.5:c.140-15509G>A	ENSP00000364797.1:n.140-15509G>A
ENST00000375664.8:c.140-15509G>A	ENSP00000364816.3:n.140-15509G>A
ENST00000414108.5:c.140-15509G>A	ENSP00000415645.1:n.140-15509G>A
ENST00000420266.5:c.140-15509G>A	ENSP00000404758.1:n.140-15509G>A
ENST00000424454.5:c.*283-15509G>A	ENSP00000404125.2:n.*283-15509G>A
ENST00000428935.5:c.148-15509G>A	ENSP00000399706.2:n.148-15509G>A
ENST00000439676.5:c.140-15509G>A	ENSP00000415727.1:n.140-15509G>A
ENST00000442148.5:c.140-15509G>A	ENSP00000400848.1:n.140-15509G>A
ENST00000448193.5:c.140-15509G>A	ENSP00000395008.1:n.140-15509G>A
ENST00000628285.2:c.148-15509G>A	ENSP00000486994.1:n.148-15509G>A
NM_016628.4:c.275-15509G>A	NP_057712.2:n.275-15509G>A
NM_100264.2:c.140-15509G>A	NP_567822.1:n.140-15509G>A
NM_100486.3:c.275-15509G>A	NP_567823.1:n.275-15509G>A
XM_005252454.2:c.293-15509G>A	XP_005252511.1:n.293-15509G>A
XM_011519491.1:c.140-15509G>A	XP_011517793.1:n.140-15509G>A
XR_930491.1:n.195-15509G>A
XM_017016315.2:c.140-15509G>A	XP_016871804.1:n.140-15509G>A
XM_017016317.2:c.140-15509G>A	XP_016871806.1:n.140-15509G>A
XM_017016318.2:c.140-15509G>A	XP_016871807.1:n.140-15509G>A
XM_024448036.1:c.140-15509G>A	XP_024303804.1:n.140-15509G>A
XR_001747110.1:n.230-15509G>A
XR_930491.2:n.195-15509G>A
NM_016628.5:c.275-15509G>A MANE Select	NP_057712.2:n.275-15509G>A
NM_100264.3:c.140-15509G>A	NP_567822.1:n.140-15509G>A
NM_100486.4:c.275-15509G>A	NP_567823.1:n.275-15509G>A