Canonical Allele Identifier: CA10996230

Gene: PXDN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1665347A>C , CM000664.2:g.1665347A>C	GRCh38
NC_000002.11:g.1669119A>C , CM000664.1:g.1669119A>C	GRCh37
NC_000002.10:g.1648126A>C	NCBI36
NG_034221.1:g.84201T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_012293.3:c.1292-273T>G MANE Select	NP_036425.1:n.1292-273T>G
ENST00000252804.9:c.1292-273T>G MANE Select	ENSP00000252804.4:n.1292-273T>G
NM_012293.2:c.1292-273T>G	NP_036425.1:n.1292-273T>G
ENST00000252804.8:c.1292-273T>G	ENSP00000252804.4:n.1292-273T>G
ENST00000425171.2:c.1220-273T>G	ENSP00000398363.2:n.1220-273T>G
ENST00000433670.5:c.1279-273T>G
ENST00000467191.5:n.484-273T>G
ENST00000478155.5:n.690-273T>G
XM_005264707.2:c.1220-273T>G	XP_005264764.1:n.1220-273T>G
XM_005264707.3:c.1220-273T>G	XP_005264764.1:n.1220-273T>G
XM_011510395.1:c.1103-273T>G	XP_011508697.1:n.1103-273T>G
XM_011510396.1:c.743-273T>G	XP_011508698.1:n.743-273T>G
XM_011510397.1:c.743-273T>G	XP_011508699.1:n.743-273T>G