Canonical Allele Identifier: CA270718508

Gene: WDR72

Linked Data

• dbSNP Id: rs532598391
• gnomAD v2: 15-53942990-C-CAACAA
• gnomAD v3: 15-53650793-C-CAACAA
• gnomAD v4: 15-53650793-C-CAACAA
• MyVariant Identifiers: chr15:g.53942995_53942996insAACAA (hg19) ; chr15:g.53942990_53942991insAACAA (hg19) ; chr15:g.53650798_53650799insAACAA (hg38) ; chr15:g.53650793_53650794insAACAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.53650810_53650814dup , CM000677.2:g.53650810_53650814dup	GRCh38
NC_000015.9:g.53943007_53943011dup , CM000677.1:g.53943007_53943011dup	GRCh37
NC_000015.8:g.51730299_51730303dup	NCBI36
NG_017034.2:g.113865_113869dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360509.10:c.1962+14774_1962+14778dup MANE Select	ENSP00000353699.5:n.1962+14774_1962+14778dup
ENST00000360509.9:c.1962+14774_1962+14778dup	ENSP00000353699.5:n.1962+14774_1962+14778dup
ENST00000396328.5:c.1962+14774_1962+14778dup	ENSP00000379619.1:n.1962+14774_1962+14778dup
ENST00000557913.5:c.1953+14774_1953+14778dup	ENSP00000453378.1:n.1953+14774_1953+14778dup
ENST00000559418.5:c.1992+14774_1992+14778dup	ENSP00000452765.1:n.1992+14774_1992+14778dup
ENST00000560036.1:c.1962+14774_1962+14778dup	ENSP00000453813.1:n.1962+14774_1962+14778dup
NM_182758.3:c.1962+14774_1962+14778dup	NP_877435.3:n.1962+14774_1962+14778dup
NR_102334.1:n.2202+14774_2202+14778dup
XM_011521433.1:c.1962+14774_1962+14778dup	XP_011519735.1:n.1962+14774_1962+14778dup
XM_011521434.1:c.1962+14774_1962+14778dup	XP_011519736.1:n.1962+14774_1962+14778dup
XM_011521435.1:c.1962+14774_1962+14778dup	XP_011519737.1:n.1962+14774_1962+14778dup
XM_011521436.1:c.1944+14774_1944+14778dup	XP_011519738.1:n.1944+14774_1944+14778dup
XM_011521437.1:c.1842+14774_1842+14778dup	XP_011519739.1:n.1842+14774_1842+14778dup
XM_011521433.2:c.1962+14774_1962+14778dup	XP_011519735.1:n.1962+14774_1962+14778dup
XM_011521435.2:c.1962+14774_1962+14778dup	XP_011519737.1:n.1962+14774_1962+14778dup
XM_011521436.2:c.1944+14774_1944+14778dup	XP_011519738.1:n.1944+14774_1944+14778dup
XM_011521437.2:c.1842+14774_1842+14778dup	XP_011519739.1:n.1842+14774_1842+14778dup
XM_017022061.1:c.1962+14774_1962+14778dup	XP_016877550.1:n.1962+14774_1962+14778dup
NM_182758.4:c.1962+14774_1962+14778dup MANE Select	NP_877435.3:n.1962+14774_1962+14778dup
NR_102334.2:n.2202+14774_2202+14778dup