Canonical Allele Identifier: CA415775387

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2337968G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406529G>C , CM000663.2:g.2406529G>C	GRCh38
NC_000001.10:g.2337968G>C , CM000663.1:g.2337968G>C	GRCh37
NC_000001.9:g.2327828G>C	NCBI36
NG_008342.1:g.11043C>G
NG_016128.1:g.19755G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000288774.8:c.927C>G	ENSP00000288774.3:p.Gly309=
ENST00000447513.7:c.867C>G MANE Select	ENSP00000407922.2:p.Gly289=
ENST00000650293.1:c.821C>G
ENST00000288774.7:c.927C>G	ENSP00000288774.3:p.Gly309=
ENST00000447513.6:c.867C>G	ENSP00000407922.2:p.Gly289=
ENST00000507596.5:c.867C>G	ENSP00000424291.1:p.Gly289=
ENST00000510434.1:c.*233C>G	ENSP00000423051.1:n.*233C>G
NM_002617.3:c.867C>G	NP_002608.1:p.Gly289=
NM_153818.1:c.927C>G	NP_722540.1:p.Gly309=
XM_011541573.1:c.924C>G	XP_011539875.1:p.Gly308=
XM_011541574.1:c.492C>G	XP_011539876.1:p.Gly164=
XM_011541575.1:c.492C>G	XP_011539877.1:p.Gly164=
XR_946666.1:n.983C>G
XR_946666.2:n.932C>G
NM_001374425.1:c.924C>G	NP_001361354.1:p.Gly308=
NM_001374426.1:c.492C>G	NP_001361355.1:p.Gly164=
NM_001374427.1:c.435C>G	NP_001361356.1:p.Gly145=
NM_002617.4:c.867C>G MANE Select	NP_002608.1:p.Gly289=
NM_153818.2:c.927C>G	NP_722540.1:p.Gly309=
NR_164636.1:n.982C>G