Canonical Allele Identifier: CA337984129

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2337945A>C (hg19) ; chr1:g.2406506A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406506A>C , CM000663.2:g.2406506A>C	GRCh38
NC_000001.10:g.2337945A>C , CM000663.1:g.2337945A>C	GRCh37
NC_000001.9:g.2327805A>C	NCBI36
NG_008342.1:g.11066T>G
NG_016128.1:g.19732A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.950T>G	ENSP00000288774.3:p.Ile317Ser
ENST00000447513.7:c.890T>G MANE Select	ENSP00000407922.2:p.Ile297Ser
ENST00000650293.1:c.844T>G
ENST00000288774.7:c.950T>G	ENSP00000288774.3:p.Ile317Ser
ENST00000447513.6:c.890T>G	ENSP00000407922.2:p.Ile297Ser
ENST00000507596.5:c.890T>G	ENSP00000424291.1:p.Ile297Ser
NM_002617.3:c.890T>G	NP_002608.1:p.Ile297Ser
NM_153818.1:c.950T>G	NP_722540.1:p.Ile317Ser
XM_011541573.1:c.947T>G	XP_011539875.1:p.Ile316Ser
XM_011541574.1:c.515T>G	XP_011539876.1:p.Ile172Ser
XM_011541575.1:c.515T>G	XP_011539877.1:p.Ile172Ser
XR_946666.1:n.1006T>G
XR_946666.2:n.955T>G
NM_001374425.1:c.947T>G	NP_001361354.1:p.Ile316Ser
NM_001374426.1:c.515T>G	NP_001361355.1:p.Ile172Ser
NM_001374427.1:c.458T>G	NP_001361356.1:p.Ile153Ser
NM_002617.4:c.890T>G MANE Select	NP_002608.1:p.Ile297Ser
NM_153818.2:c.950T>G	NP_722540.1:p.Ile317Ser
NR_164636.1:n.1005T>G