Canonical Allele Identifier: CA415775452

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2338161G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406722G>C , CM000663.2:g.2406722G>C	GRCh38
NC_000001.10:g.2338161G>C , CM000663.1:g.2338161G>C	GRCh37
NC_000001.9:g.2328021G>C	NCBI36
NG_008342.1:g.10850C>G
NG_016128.1:g.19948G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.834C>G	ENSP00000288774.3:p.Arg278=
ENST00000447513.7:c.774C>G MANE Select	ENSP00000407922.2:p.Arg258=
ENST00000650293.1:c.728C>G
ENST00000288774.7:c.834C>G	ENSP00000288774.3:p.Arg278=
ENST00000447513.6:c.774C>G	ENSP00000407922.2:p.Arg258=
ENST00000507596.5:c.774C>G	ENSP00000424291.1:p.Arg258=
ENST00000510434.1:c.*140C>G	ENSP00000423051.1:n.*140C>G
NM_002617.3:c.774C>G	NP_002608.1:p.Arg258=
NM_153818.1:c.834C>G	NP_722540.1:p.Arg278=
XM_011541573.1:c.831C>G	XP_011539875.1:p.Arg277=
XM_011541574.1:c.399C>G	XP_011539876.1:p.Arg133=
XM_011541575.1:c.399C>G	XP_011539877.1:p.Arg133=
XR_946666.1:n.890C>G
XR_946666.2:n.839C>G
NM_001374425.1:c.831C>G	NP_001361354.1:p.Arg277=
NM_001374426.1:c.399C>G	NP_001361355.1:p.Arg133=
NM_001374427.1:c.342C>G	NP_001361356.1:p.Arg114=
NM_002617.4:c.774C>G MANE Select	NP_002608.1:p.Arg258=
NM_153818.2:c.834C>G	NP_722540.1:p.Arg278=
NR_164636.1:n.889C>G