Canonical Allele Identifier: CA1513198

Gene: PXDN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1660882A>G , CM000664.2:g.1660882A>G	GRCh38
NC_000002.11:g.1664654A>G , CM000664.1:g.1664654A>G	GRCh37
NC_000002.10:g.1643661A>G	NCBI36
NG_034221.1:g.88666T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425171.2:c.1764T>C	ENSP00000398363.2:p.Asn588=
ENST00000252804.9:c.1836T>C MANE Select	ENSP00000252804.4:p.Asn612=
ENST00000252804.8:c.1836T>C	ENSP00000252804.4:p.Asn612=
ENST00000433670.5:c.1823T>C
ENST00000478155.5:n.2428T>C
NM_012293.2:c.1836T>C	NP_036425.1:p.Asn612=
XM_005264707.2:c.1764T>C	XP_005264764.1:p.Asn588=
XM_011510395.1:c.1647T>C	XP_011508697.1:p.Asn549=
XM_011510396.1:c.1287T>C	XP_011508698.1:p.Asn429=
XM_011510397.1:c.1287T>C	XP_011508699.1:p.Asn429=
XM_005264707.3:c.1764T>C	XP_005264764.1:p.Asn588=
NM_012293.3:c.1836T>C MANE Select	NP_036425.1:p.Asn612=