Canonical Allele Identifier: CA206978914

Gene: WDFY4

Linked Data

• dbSNP Id: rs11101442
• gnomAD v2: 10-49936336-C-A
• gnomAD v3: 10-48728291-C-A
• gnomAD v4: 10-48728291-C-A
• MyVariant Identifiers: chr10:g.49936336C>A (hg19) ; chr10:g.48728291C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.48728291C>A , CM000672.2:g.48728291C>A	GRCh38
NC_000010.10:g.49936336C>A , CM000672.1:g.49936336C>A	GRCh37
NC_000010.9:g.49606342C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000325239.12:c.971+632C>A MANE Select	ENSP00000320563.5:n.971+632C>A
ENST00000325239.11:c.971+632C>A	ENSP00000320563.5:n.971+632C>A
ENST00000325239.9:c.971+632C>A	ENSP00000320563.5:n.971+632C>A
ENST00000360890.6:c.971+632C>A	ENSP00000354141.2:n.971+632C>A
NM_020945.1:c.971+632C>A	NP_065996.1:n.971+632C>A
XM_005270004.2:c.971+632C>A	XP_005270061.1:n.971+632C>A
XM_011539986.1:c.971+632C>A	XP_011538288.1:n.971+632C>A
XM_011539987.1:c.971+632C>A	XP_011538289.1:n.971+632C>A
XM_011539988.1:c.971+632C>A	XP_011538290.1:n.971+632C>A
XM_011539989.1:c.1091+632C>A	XP_011538291.1:n.1091+632C>A
XM_011539990.1:c.1091+632C>A	XP_011538292.1:n.1091+632C>A
XM_011539991.1:c.1091+632C>A	XP_011538293.1:n.1091+632C>A
XM_011539992.1:c.1091+632C>A	XP_011538294.1:n.1091+632C>A
XM_005270004.3:c.971+632C>A	XP_005270061.1:n.971+632C>A
XM_011539986.3:c.1091+632C>A	XP_011538288.2:n.1091+632C>A
XM_011539987.2:c.1091+632C>A	XP_011538289.2:n.1091+632C>A
XM_011539988.2:c.971+632C>A	XP_011538290.1:n.971+632C>A
XM_011539990.3:c.1091+632C>A	XP_011538292.1:n.1091+632C>A
XM_011539991.3:c.1091+632C>A	XP_011538293.1:n.1091+632C>A
XM_011539992.2:c.1091+632C>A	XP_011538294.1:n.1091+632C>A
XM_017016463.1:c.971+632C>A	XP_016871952.1:n.971+632C>A
XM_017016465.2:c.971+632C>A	XP_016871954.1:n.971+632C>A
NM_001370153.1:c.971+632C>A	NP_001357082.1:n.971+632C>A
NM_001370154.1:c.971+632C>A	NP_001357083.1:n.971+632C>A
NM_020945.2:c.971+632C>A	NP_065996.1:n.971+632C>A
NM_001394531.1:c.971+632C>A MANE Select	NP_001381460.1:n.971+632C>A