Canonical Allele Identifier: CA2704344341

Gene: WDR49

Linked Data

• dbSNP Id: rs147857451

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.167631026_167631028dup , CM000665.2:g.167631026_167631028dup	GRCh38
NC_000003.11:g.167348814_167348816dup , CM000665.1:g.167348814_167348816dup	GRCh37
NC_000003.10:g.168831508_168831510dup	NCBI36
NG_053014.1:g.31979_31981dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647816.2:c.166-3733_166-3731dup	ENSP00000497120.1:n.166-3733_166-3731dup
ENST00000682715.1:c.166-3733_166-3731dup MANE Select	ENSP00000507497.1:n.166-3733_166-3731dup
ENST00000647816.1:c.166-3733_166-3731dup	ENSP00000497120.1:n.166-3733_166-3731dup
ENST00000308378.7:c.-66+22236_-66+22238dup	ENSP00000311343.3:n.-66+22236_-66+22238dup
ENST00000460448.5:c.165+22236_165+22238dup	ENSP00000417090.1:n.165+22236_165+22238dup
ENST00000466760.5:c.165+22236_165+22238dup	ENSP00000418718.1:n.165+22236_165+22238dup
ENST00000471198.1:n.410+2384_410+2386dup
ENST00000479765.5:c.166-3733_166-3731dup	ENSP00000419749.1:n.166-3733_166-3731dup
ENST00000488012.5:c.166-9382_166-9380dup	ENSP00000419917.1:n.166-9382_166-9380dup
NM_178824.3:c.-66+22236_-66+22238dup	NP_849146.1:n.-66+22236_-66+22238dup
NM_001348951.1:c.166-3733_166-3731dup	NP_001335880.1:n.166-3733_166-3731dup
NM_001348952.1:c.166-3733_166-3731dup	NP_001335881.1:n.166-3733_166-3731dup
NM_001366157.1:c.166-3733_166-3731dup MANE Select	NP_001353086.1:n.166-3733_166-3731dup
NM_001366158.1:c.-66+22236_-66+22238dup	NP_001353087.1:n.-66+22236_-66+22238dup
NM_001348951.2:c.166-3733_166-3731dup	NP_001335880.1:n.166-3733_166-3731dup
NM_001348952.2:c.166-3733_166-3731dup	NP_001335881.1:n.166-3733_166-3731dup