Canonical Allele Identifier: CA2048891688

Gene: PAWR

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.79668450A= , CM000674.2:g.79668450A=	GRCh38
NC_000012.11:g.80062230A= , CM000674.1:g.80062230A=	GRCh37
NC_000012.10:g.78586361A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328827.9:c.516+21279T= MANE Select	ENSP00000328088.4:n.516+21279T=
ENST00000328827.8:c.516+21279T=	ENSP00000328088.4:n.516+21279T=
ENST00000547571.1:n.303-42T=
ENST00000550006.1:n.329+21279T=
ENST00000551712.1:c.352+21279T=
NM_002583.2:c.516+21279T=	NP_002574.2:n.516+21279T=
XM_006719435.2:c.516+21279T=	XP_006719498.1:n.516+21279T=
XM_006719436.2:c.516+21279T=	XP_006719499.1:n.516+21279T=
XR_944560.1:n.826-42T=
XR_944561.1:n.826-42T=
NM_001354732.1:c.516+21279T=	NP_001341661.1:n.516+21279T=
NM_001354733.1:c.516+21279T=	NP_001341662.1:n.516+21279T=
NM_002583.3:c.516+21279T=	NP_002574.2:n.516+21279T=
XM_017019378.1:c.516+21279T=	XP_016874867.1:n.516+21279T=
XM_017019379.1:c.517-42T=	XP_016874868.1:n.517-42T=
XR_944560.2:n.890-42T=
XR_944561.2:n.890-42T=
NM_002583.4:c.516+21279T= MANE Select	NP_002574.2:n.516+21279T=
NM_001354732.2:c.516+21279T=	NP_001341661.1:n.516+21279T=
NM_001354733.2:c.516+21279T=	NP_001341662.1:n.516+21279T=