Canonical Allele Identifier: CA2048871569

Gene: PAWR

Linked Data

• dbSNP Id: rs7305141

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.79621793G>T , CM000674.2:g.79621793G>T	GRCh38
NC_000012.11:g.80015573G>T , CM000674.1:g.80015573G>T	GRCh37
NC_000012.10:g.78539704G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000328827.9:c.517-586C>A MANE Select	ENSP00000328088.4:n.517-586C>A
ENST00000328827.8:c.517-586C>A	ENSP00000328088.4:n.517-586C>A
ENST00000549050.1:n.57+10313C>A
ENST00000550006.1:n.401-586C>A
ENST00000551712.1:c.353-586C>A
NM_002583.2:c.517-586C>A	NP_002574.2:n.517-586C>A
XM_006719435.2:c.517-586C>A	XP_006719498.1:n.517-586C>A
XM_006719436.2:c.517-586C>A	XP_006719499.1:n.517-586C>A
NM_001354732.1:c.517-586C>A	NP_001341661.1:n.517-586C>A
NM_001354733.1:c.517-586C>A	NP_001341662.1:n.517-586C>A
NM_002583.3:c.517-586C>A	NP_002574.2:n.517-586C>A
XM_017019378.1:c.517-586C>A	XP_016874867.1:n.517-586C>A
NM_002583.4:c.517-586C>A MANE Select	NP_002574.2:n.517-586C>A
NM_001354732.2:c.517-586C>A	NP_001341661.1:n.517-586C>A
NM_001354733.2:c.517-586C>A	NP_001341662.1:n.517-586C>A