Canonical Allele Identifier: CA1585703898

Gene: WNT8A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138084300C= , CM000667.2:g.138084300C=	GRCh38
NC_000005.9:g.137419989C= , CM000667.1:g.137419989C=	GRCh37
NC_000005.8:g.137447888C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001300939.2:c.156+17C= MANE Select	NP_001287868.1:n.156+17C=
ENST00000506684.6:c.156+17C= MANE Select	ENSP00000426653.1:n.156+17C=
NM_001300938.1:c.156+17C=	NP_001287867.1:n.156+17C=
NM_001300938.2:c.156+17C=	NP_001287867.1:n.156+17C=
NM_001300939.1:c.156+17C=	NP_001287868.1:n.156+17C=
NM_058244.3:c.102+17C=	NP_490645.1:n.102+17C=
NM_058244.4:c.102+17C=	NP_490645.1:n.102+17C=
NR_125351.1:n.300+17C=
NR_125351.2:n.159+17C=
ENST00000361560.6:c.102+17C=	ENSP00000354726.2:n.102+17C=
ENST00000398754.1:c.102+17C=	ENSP00000381739.1:n.102+17C=
ENST00000504809.5:c.156+17C=	ENSP00000424809.1:n.156+17C=
ENST00000506684.5:c.156+17C=	ENSP00000426653.1:n.156+17C=
XM_011543625.1:c.156+17C=	XP_011541927.1:n.156+17C=
XM_011543625.2:c.222+17C=	XP_011541927.2:n.222+17C=
XM_017009824.1:c.222+17C=	XP_016865313.1:n.222+17C=
XM_017009825.1:c.222+17C=	XP_016865314.1:n.222+17C=
XM_017009826.1:c.-187+17C=	XP_016865315.1:n.-187+17C=
XR_948295.1:n.257+17C=