Canonical Allele Identifier: CA415775987

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2340245C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408806C>A , CM000663.2:g.2408806C>A	GRCh38
NC_000001.10:g.2340245C>A , CM000663.1:g.2340245C>A	GRCh37
NC_000001.9:g.2330105C>A	NCBI36
NG_008342.1:g.8766G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.246G>T	ENSP00000288774.3:p.Ser82=
ENST00000447513.7:c.246G>T MANE Select	ENSP00000407922.2:p.Ser82=
ENST00000650293.1:c.200G>T
ENST00000288774.7:c.246G>T	ENSP00000288774.3:p.Ser82=
ENST00000447513.6:c.246G>T	ENSP00000407922.2:p.Ser82=
ENST00000502666.1:c.451G>T	ENSP00000461951.1:n.451G>T
ENST00000507596.5:c.246G>T	ENSP00000424291.1:p.Ser82=
ENST00000508384.5:c.-187G>T	ENSP00000464289.1:n.-187G>T
ENST00000510434.1:c.246G>T	ENSP00000423051.1:p.Ser82=
ENST00000514502.1:c.*263G>T	ENSP00000425924.1:n.*263G>T
ENST00000515760.1:n.380G>T
NM_002617.3:c.246G>T	NP_002608.1:p.Ser82=
NM_153818.1:c.246G>T	NP_722540.1:p.Ser82=
XM_011541573.1:c.246G>T	XP_011539875.1:p.Ser82=
XM_011541574.1:c.-187G>T	XP_011539876.1:n.-187G>T
XM_011541575.1:c.-187G>T	XP_011539877.1:n.-187G>T
XM_011541576.1:c.246G>T	XP_011539878.1:p.Ser82=
XR_946666.1:n.366G>T
XM_011541576.2:c.246G>T	XP_011539878.1:p.Ser82=
XR_946666.2:n.315G>T
NM_001374425.1:c.246G>T	NP_001361354.1:p.Ser82=
NM_001374426.1:c.-187G>T	NP_001361355.1:n.-187G>T
NM_001374427.1:c.-187G>T	NP_001361356.1:n.-187G>T
NM_002617.4:c.246G>T MANE Select	NP_002608.1:p.Ser82=
NM_153818.2:c.246G>T	NP_722540.1:p.Ser82=
NR_164636.1:n.365G>T