Canonical Allele Identifier: CA397593451

Gene: WDR81

Linked Data

• MyVariant Identifiers: chr17:g.1631479C>G (hg19) ; chr17:g.1728185C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1728185C>G , CM000679.2:g.1728185C>G	GRCh38
NC_000017.10:g.1631479C>G , CM000679.1:g.1631479C>G	GRCh37
NC_000017.9:g.1578229C>G	NCBI36
NG_032811.1:g.16663C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409644.6:c.3226C>G MANE Select	ENSP00000386609.1:p.Gln1076Glu
ENST00000309182.9:c.73C>G	ENSP00000312074.5:p.Gln25Glu
ENST00000409644.5:c.3226C>G	ENSP00000386609.1:p.Gln1076Glu
ENST00000418841.5:c.-89+3399C>G	ENSP00000395198.1:n.-89+3399C>G
ENST00000419248.5:c.-14-2195C>G	ENSP00000407845.1:n.-14-2195C>G
ENST00000437219.6:c.59-2195C>G	ENSP00000391074.2:n.59-2195C>G
ENST00000446363.5:c.-308-2570C>G	ENSP00000401560.1:n.-308-2570C>G
ENST00000455636.5:c.59-2195C>G	ENSP00000395226.1:n.59-2195C>G
ENST00000464528.5:n.612C>G
ENST00000468539.5:c.63-4140C>G	ENSP00000460742.1:n.63-4140C>G
ENST00000492901.1:n.88-2195C>G
NM_001163673.1:c.59-2195C>G	NP_001157145.1:n.59-2195C>G
NM_001163809.1:c.3226C>G	NP_001157281.1:p.Gln1076Glu
NM_001163811.1:c.-14-2195C>G	NP_001157283.1:n.-14-2195C>G
NM_152348.3:c.73C>G	NP_689561.2:p.Gln25Glu
XM_005256454.2:c.3226C>G	XP_005256511.1:p.Gln1076Glu
XM_011523650.1:c.3226C>G	XP_011521952.1:p.Gln1076Glu
XM_011523651.1:c.73C>G	XP_011521953.1:p.Gln25Glu
XR_933973.1:n.3370C>G
XM_011523651.2:c.73C>G	XP_011521953.1:p.Gln25Glu
XM_017024184.1:c.3226C>G	XP_016879673.1:p.Gln1076Glu
XR_001752427.1:n.3378C>G
XR_933973.2:n.3378C>G
NM_001163809.2:c.3226C>G MANE Select	NP_001157281.1:p.Gln1076Glu
NM_001163811.2:c.-14-2195C>G	NP_001157283.1:n.-14-2195C>G
NM_152348.4:c.73C>G	NP_689561.2:p.Gln25Glu
NM_001163673.2:c.59-2195C>G	NP_001157145.1:n.59-2195C>G