Canonical Allele Identifier: CA713831247

Gene: WDR72

Linked Data

• dbSNP Id: rs1229070123
• gnomAD v3: 15-53650746-G-A
• gnomAD v4: 15-53650746-G-A
• MyVariant Identifiers: chr15:g.53942943G>A (hg19) ; chr15:g.53650746G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.53650746G>A , CM000677.2:g.53650746G>A	GRCh38
NC_000015.9:g.53942943G>A , CM000677.1:g.53942943G>A	GRCh37
NC_000015.8:g.51730235G>A	NCBI36
NG_017034.2:g.113917C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360509.10:c.1962+14826C>T MANE Select	ENSP00000353699.5:n.1962+14826C>T
ENST00000360509.9:c.1962+14826C>T	ENSP00000353699.5:n.1962+14826C>T
ENST00000396328.5:c.1962+14826C>T	ENSP00000379619.1:n.1962+14826C>T
ENST00000557913.5:c.1953+14826C>T	ENSP00000453378.1:n.1953+14826C>T
ENST00000559418.5:c.1992+14826C>T	ENSP00000452765.1:n.1992+14826C>T
ENST00000560036.1:c.1962+14826C>T	ENSP00000453813.1:n.1962+14826C>T
NM_182758.3:c.1962+14826C>T	NP_877435.3:n.1962+14826C>T
NR_102334.1:n.2202+14826C>T
XM_011521433.1:c.1962+14826C>T	XP_011519735.1:n.1962+14826C>T
XM_011521434.1:c.1962+14826C>T	XP_011519736.1:n.1962+14826C>T
XM_011521435.1:c.1962+14826C>T	XP_011519737.1:n.1962+14826C>T
XM_011521436.1:c.1944+14826C>T	XP_011519738.1:n.1944+14826C>T
XM_011521437.1:c.1842+14826C>T	XP_011519739.1:n.1842+14826C>T
XM_011521433.2:c.1962+14826C>T	XP_011519735.1:n.1962+14826C>T
XM_011521435.2:c.1962+14826C>T	XP_011519737.1:n.1962+14826C>T
XM_011521436.2:c.1944+14826C>T	XP_011519738.1:n.1944+14826C>T
XM_011521437.2:c.1842+14826C>T	XP_011519739.1:n.1842+14826C>T
XM_017022061.1:c.1962+14826C>T	XP_016877550.1:n.1962+14826C>T
NM_182758.4:c.1962+14826C>T MANE Select	NP_877435.3:n.1962+14826C>T
NR_102334.2:n.2202+14826C>T