Canonical Allele Identifier: CA206516730

Gene: WDFY4

Linked Data

• dbSNP Id: rs766927925
• gnomAD v2: 10-49985204-C-T
• gnomAD v3: 10-48777159-C-T
• gnomAD v4: 10-48777159-C-T
• MyVariant Identifiers: chr10:g.49985204C>T (hg19) ; chr10:g.48777159C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.48777159C>T , CM000672.2:g.48777159C>T	GRCh38
NC_000010.10:g.49985204C>T , CM000672.1:g.49985204C>T	GRCh37
NC_000010.9:g.49655210C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325239.12:c.3098+175C>T MANE Select	ENSP00000320563.5:n.3098+175C>T
ENST00000325239.11:c.3098+175C>T	ENSP00000320563.5:n.3098+175C>T
ENST00000325239.9:c.3098+175C>T	ENSP00000320563.5:n.3098+175C>T
NM_020945.1:c.3098+175C>T	NP_065996.1:n.3098+175C>T
XM_005270004.2:c.3098+175C>T	XP_005270061.1:n.3098+175C>T
XM_011539986.1:c.3098+175C>T	XP_011538288.1:n.3098+175C>T
XM_011539987.1:c.3098+175C>T	XP_011538289.1:n.3098+175C>T
XM_011539988.1:c.3098+175C>T	XP_011538290.1:n.3098+175C>T
XM_011539989.1:c.3218+175C>T	XP_011538291.1:n.3218+175C>T
XM_011539990.1:c.3218+175C>T	XP_011538292.1:n.3218+175C>T
XM_011539991.1:c.3218+175C>T	XP_011538293.1:n.3218+175C>T
XM_011539992.1:c.3218+175C>T	XP_011538294.1:n.3218+175C>T
XM_005270004.3:c.3098+175C>T	XP_005270061.1:n.3098+175C>T
XM_011539986.3:c.3218+175C>T	XP_011538288.2:n.3218+175C>T
XM_011539987.2:c.3218+175C>T	XP_011538289.2:n.3218+175C>T
XM_011539988.2:c.3098+175C>T	XP_011538290.1:n.3098+175C>T
XM_011539990.3:c.3218+175C>T	XP_011538292.1:n.3218+175C>T
XM_011539991.3:c.3218+175C>T	XP_011538293.1:n.3218+175C>T
XM_011539992.2:c.3218+175C>T	XP_011538294.1:n.3218+175C>T
XM_017016463.1:c.3098+175C>T	XP_016871952.1:n.3098+175C>T
XM_017016465.2:c.3098+175C>T	XP_016871954.1:n.3098+175C>T
NM_001370153.1:c.3098+175C>T	NP_001357082.1:n.3098+175C>T
NM_020945.2:c.3098+175C>T	NP_065996.1:n.3098+175C>T
NM_001394531.1:c.3098+175C>T MANE Select	NP_001381460.1:n.3098+175C>T