Canonical Allele Identifier: CA415775379

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2337944G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406505G>T , CM000663.2:g.2406505G>T	GRCh38
NC_000001.10:g.2337944G>T , CM000663.1:g.2337944G>T	GRCh37
NC_000001.9:g.2327804G>T	NCBI36
NG_008342.1:g.11067C>A
NG_016128.1:g.19731G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.951C>A	ENSP00000288774.3:p.Ile317=
ENST00000447513.7:c.891C>A MANE Select	ENSP00000407922.2:p.Ile297=
ENST00000650293.1:c.845C>A
ENST00000288774.7:c.951C>A	ENSP00000288774.3:p.Ile317=
ENST00000447513.6:c.891C>A	ENSP00000407922.2:p.Ile297=
ENST00000507596.5:c.891C>A	ENSP00000424291.1:p.Ile297=
NM_002617.3:c.891C>A	NP_002608.1:p.Ile297=
NM_153818.1:c.951C>A	NP_722540.1:p.Ile317=
XM_011541573.1:c.948C>A	XP_011539875.1:p.Ile316=
XM_011541574.1:c.516C>A	XP_011539876.1:p.Ile172=
XM_011541575.1:c.516C>A	XP_011539877.1:p.Ile172=
XR_946666.1:n.1007C>A
XR_946666.2:n.956C>A
NM_001374425.1:c.948C>A	NP_001361354.1:p.Ile316=
NM_001374426.1:c.516C>A	NP_001361355.1:p.Ile172=
NM_001374427.1:c.459C>A	NP_001361356.1:p.Ile153=
NM_002617.4:c.891C>A MANE Select	NP_002608.1:p.Ile297=
NM_153818.2:c.951C>A	NP_722540.1:p.Ile317=
NR_164636.1:n.1006C>A