Canonical Allele Identifier: CA337988891

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2340229A>C (hg19) ; chr1:g.2408790A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408790A>C , CM000663.2:g.2408790A>C	GRCh38
NC_000001.10:g.2340229A>C , CM000663.1:g.2340229A>C	GRCh37
NC_000001.9:g.2330089A>C	NCBI36
NG_008342.1:g.8782T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.262T>G	ENSP00000288774.3:p.Ser88Ala
ENST00000447513.7:c.262T>G MANE Select	ENSP00000407922.2:p.Ser88Ala
ENST00000650293.1:c.216T>G
ENST00000288774.7:c.262T>G	ENSP00000288774.3:p.Ser88Ala
ENST00000447513.6:c.262T>G	ENSP00000407922.2:p.Ser88Ala
ENST00000502666.1:c.467T>G	ENSP00000461951.1:n.467T>G
ENST00000507596.5:c.262T>G	ENSP00000424291.1:p.Ser88Ala
ENST00000508384.5:c.-171T>G	ENSP00000464289.1:n.-171T>G
ENST00000510434.1:c.262T>G	ENSP00000423051.1:p.Ser88Ala
ENST00000514502.1:c.*279T>G	ENSP00000425924.1:n.*279T>G
ENST00000515760.1:n.396T>G
NM_002617.3:c.262T>G	NP_002608.1:p.Ser88Ala
NM_153818.1:c.262T>G	NP_722540.1:p.Ser88Ala
XM_011541573.1:c.262T>G	XP_011539875.1:p.Ser88Ala
XM_011541574.1:c.-171T>G	XP_011539876.1:n.-171T>G
XM_011541575.1:c.-171T>G	XP_011539877.1:n.-171T>G
XM_011541576.1:c.262T>G	XP_011539878.1:p.Ser88Ala
XR_946666.1:n.382T>G
XM_011541576.2:c.262T>G	XP_011539878.1:p.Ser88Ala
XR_946666.2:n.331T>G
NM_001374425.1:c.262T>G	NP_001361354.1:p.Ser88Ala
NM_001374426.1:c.-171T>G	NP_001361355.1:n.-171T>G
NM_001374427.1:c.-171T>G	NP_001361356.1:n.-171T>G
NM_002617.4:c.262T>G MANE Select	NP_002608.1:p.Ser88Ala
NM_153818.2:c.262T>G	NP_722540.1:p.Ser88Ala
NR_164636.1:n.381T>G