Canonical Allele Identifier: CA415775392

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2337974G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406535G>C , CM000663.2:g.2406535G>C	GRCh38
NC_000001.10:g.2337974G>C , CM000663.1:g.2337974G>C	GRCh37
NC_000001.9:g.2327834G>C	NCBI36
NG_008342.1:g.11037C>G
NG_016128.1:g.19761G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.921C>G	ENSP00000288774.3:p.Pro307=
ENST00000447513.7:c.861C>G MANE Select	ENSP00000407922.2:p.Pro287=
ENST00000650293.1:c.815C>G
ENST00000288774.7:c.921C>G	ENSP00000288774.3:p.Pro307=
ENST00000447513.6:c.861C>G	ENSP00000407922.2:p.Pro287=
ENST00000507596.5:c.861C>G	ENSP00000424291.1:p.Pro287=
ENST00000510434.1:c.*227C>G	ENSP00000423051.1:n.*227C>G
NM_002617.3:c.861C>G	NP_002608.1:p.Pro287=
NM_153818.1:c.921C>G	NP_722540.1:p.Pro307=
XM_011541573.1:c.918C>G	XP_011539875.1:p.Pro306=
XM_011541574.1:c.486C>G	XP_011539876.1:p.Pro162=
XM_011541575.1:c.486C>G	XP_011539877.1:p.Pro162=
XR_946666.1:n.977C>G
XR_946666.2:n.926C>G
NM_001374425.1:c.918C>G	NP_001361354.1:p.Pro306=
NM_001374426.1:c.486C>G	NP_001361355.1:p.Pro162=
NM_001374427.1:c.429C>G	NP_001361356.1:p.Pro143=
NM_002617.4:c.861C>G MANE Select	NP_002608.1:p.Pro287=
NM_153818.2:c.921C>G	NP_722540.1:p.Pro307=
NR_164636.1:n.976C>G