Canonical Allele Identifier: CA11054191

Gene: PXDN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1638681T>C , CM000664.2:g.1638681T>C	GRCh38
NC_000002.11:g.1642453T>C , CM000664.1:g.1642453T>C	GRCh37
NC_000002.10:g.1621460T>C	NCBI36
NG_034221.1:g.110867A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_012293.3:c.4206+165A>G MANE Select	NP_036425.1:n.4206+165A>G
ENST00000252804.9:c.4206+165A>G MANE Select	ENSP00000252804.4:n.4206+165A>G
NM_012293.2:c.4206+165A>G	NP_036425.1:n.4206+165A>G
ENST00000252804.8:c.4206+165A>G	ENSP00000252804.4:n.4206+165A>G
ENST00000453308.1:c.225+621A>G
ENST00000478155.5:n.3294+165A>G
XM_005264707.2:c.4134+165A>G	XP_005264764.1:n.4134+165A>G
XM_005264707.3:c.4134+165A>G	XP_005264764.1:n.4134+165A>G
XM_011510395.1:c.4017+165A>G	XP_011508697.1:n.4017+165A>G
XM_011510396.1:c.3657+165A>G	XP_011508698.1:n.3657+165A>G
XM_011510397.1:c.3657+165A>G	XP_011508699.1:n.3657+165A>G