Canonical Allele Identifier: CA2499214623

Gene: PEX10

Linked Data

• ClinVar Variation Id: 1159000
• ClinVar RCV Id: RCV001502594
• dbSNP Id: rs778931694

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408862C>A , CM000663.2:g.2408862C>A	GRCh38
NC_000001.10:g.2340301C>A , CM000663.1:g.2340301C>A	GRCh37
NC_000001.9:g.2330161C>A	NCBI36
NG_008342.1:g.8710G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.194-4G>T	ENSP00000288774.3:n.194-4G>T
ENST00000447513.7:c.194-4G>T MANE Select	ENSP00000407922.2:n.194-4G>T
ENST00000650293.1:c.148-4G>T
ENST00000288774.7:c.194-4G>T	ENSP00000288774.3:n.194-4G>T
ENST00000447513.6:c.194-4G>T	ENSP00000407922.2:n.194-4G>T
ENST00000502666.1:c.399-4G>T	ENSP00000461951.1:n.399-4G>T
ENST00000507596.5:c.194-4G>T	ENSP00000424291.1:n.194-4G>T
ENST00000508384.5:c.-239-4G>T	ENSP00000464289.1:n.-239-4G>T
ENST00000510434.1:c.194-4G>T	ENSP00000423051.1:n.194-4G>T
ENST00000514502.1:c.*211-4G>T	ENSP00000425924.1:n.*211-4G>T
ENST00000515760.1:n.328-4G>T
NM_002617.3:c.194-4G>T	NP_002608.1:n.194-4G>T
NM_153818.1:c.194-4G>T	NP_722540.1:n.194-4G>T
XM_011541573.1:c.194-4G>T	XP_011539875.1:n.194-4G>T
XM_011541574.1:c.-239-4G>T	XP_011539876.1:n.-239-4G>T
XM_011541575.1:c.-239-4G>T	XP_011539877.1:n.-239-4G>T
XM_011541576.1:c.194-4G>T	XP_011539878.1:n.194-4G>T
XR_946666.1:n.314-4G>T
XM_011541576.2:c.194-4G>T	XP_011539878.1:n.194-4G>T
XR_946666.2:n.263-4G>T
NM_001374425.1:c.194-4G>T	NP_001361354.1:n.194-4G>T
NM_001374426.1:c.-239-4G>T	NP_001361355.1:n.-239-4G>T
NM_001374427.1:c.-239-4G>T	NP_001361356.1:n.-239-4G>T
NM_002617.4:c.194-4G>T MANE Select	NP_002608.1:n.194-4G>T
NM_153818.2:c.194-4G>T	NP_722540.1:n.194-4G>T
NR_164636.1:n.313-4G>T