Canonical Allele Identifier: CA11054195

Gene: PXDN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1639684T>C , CM000664.2:g.1639684T>C	GRCh38
NC_000002.11:g.1643456T>C , CM000664.1:g.1643456T>C	GRCh37
NC_000002.10:g.1622463T>C	NCBI36
NG_034221.1:g.109864A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_012293.3:c.3953-262A>G MANE Select	NP_036425.1:n.3953-262A>G
ENST00000252804.9:c.3953-262A>G MANE Select	ENSP00000252804.4:n.3953-262A>G
NM_012293.2:c.3953-262A>G	NP_036425.1:n.3953-262A>G
ENST00000252804.8:c.3953-262A>G	ENSP00000252804.4:n.3953-262A>G
ENST00000453308.1:c.105-262A>G
ENST00000478155.5:n.3041-262A>G
XM_005264707.2:c.3881-262A>G	XP_005264764.1:n.3881-262A>G
XM_005264707.3:c.3881-262A>G	XP_005264764.1:n.3881-262A>G
XM_011510395.1:c.3764-262A>G	XP_011508697.1:n.3764-262A>G
XM_011510396.1:c.3404-262A>G	XP_011508698.1:n.3404-262A>G
XM_011510397.1:c.3404-262A>G	XP_011508699.1:n.3404-262A>G