Canonical Allele Identifier: CA8773784

Gene: WBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75846959G>A , CM000679.2:g.75846959G>A	GRCh38
NC_000017.10:g.73843040G>A , CM000679.1:g.73843040G>A	GRCh37
NC_000017.9:g.71354635G>A	NCBI36
NG_007266.1:g.2759C>T , LRG_122:g.2759C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254806.8:c.681C>T MANE Select	ENSP00000254806.3:p.Ala227=
ENST00000254806.7:c.681C>T	ENSP00000254806.3:p.Ala227=
ENST00000433525.6:c.546C>T	ENSP00000415251.2:p.Ala182=
ENST00000585462.5:c.615C>T	ENSP00000467583.1:p.Ala205=
ENST00000586257.5:c.377C>T
ENST00000587642.5:n.2623C>T
ENST00000588373.5:c.*738C>T	ENSP00000465052.1:n.*738C>T
ENST00000589236.1:n.681C>T
ENST00000590221.5:c.669C>T	ENSP00000466450.1:p.Ala223=
ENST00000591399.5:c.681C>T	ENSP00000467579.1:p.Ala227=
ENST00000591831.5:c.656-172C>T	ENSP00000466999.1:n.656-172C>T
ENST00000626827.2:c.656-172C>T	ENSP00000486675.1:n.656-172C>T
NM_012478.3:c.681C>T	NP_036610.2:p.Ala227=
XM_011524579.1:c.615C>T	XP_011522881.1:p.Ala205=
XM_011524580.1:c.546C>T	XP_011522882.1:p.Ala182=
NM_001330499.1:c.546C>T	NP_001317428.1:p.Ala182=
NM_001348170.1:c.681C>T	NP_001335099.1:p.Ala227=
NM_012478.4:c.681C>T MANE Select	NP_036610.2:p.Ala227=
NM_001330499.2:c.546C>T	NP_001317428.1:p.Ala182=