Canonical Allele Identifier: CA2048891690

Gene: PAWR

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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