Canonical Allele Identifier: CA1512860
Gene: PXDN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.1648888G>A , CM000664.2:g.1648888G>A GRCh38
NC_000002.11:g.1652660G>A , CM000664.1:g.1652660G>A GRCh37
NC_000002.10:g.1631667G>A NCBI36
NG_034221.1:g.100660C>T

Transcript Alleles

HGVS Amino-acid Change
NM_012293.3:c.2892C>T MANE Select NP_036425.1:p.Asn964=
ENST00000252804.9:c.2892C>T MANE Select ENSP00000252804.4:p.Asn964=
NM_012293.2:c.2892C>T NP_036425.1:p.Asn964=
ENST00000252804.8:c.2892C>T ENSP00000252804.4:p.Asn964=
ENST00000478155.5:n.2697-4136C>T
XM_005264707.2:c.2820C>T XP_005264764.1:p.Asn940=
XM_005264707.3:c.2820C>T XP_005264764.1:p.Asn940=
XM_011510395.1:c.2703C>T XP_011508697.1:p.Asn901=
XM_011510396.1:c.2343C>T XP_011508698.1:p.Asn781=
XM_011510397.1:c.2343C>T XP_011508699.1:p.Asn781=