Canonical Allele Identifier: CA2742186697
Gene: PEX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2408877_2408878insACA , CM000663.2:g.2408877_2408878insACA GRCh38
NC_000001.10:g.2340316_2340317insACA , CM000663.1:g.2340316_2340317insACA GRCh37
NC_000001.9:g.2330176_2330177insACA NCBI36
NG_008342.1:g.8694_8695insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000288774.8:c.194-20_194-19insTGT ENSP00000288774.3:n.194-20_194-19insTGT
ENST00000447513.7:c.194-20_194-19insTGT MANE Select ENSP00000407922.2:n.194-20_194-19insTGT
ENST00000650293.1:c.148-20_148-19insTGT
ENST00000288774.7:c.194-20_194-19insTGT ENSP00000288774.3:n.194-20_194-19insTGT
ENST00000447513.6:c.194-20_194-19insTGT ENSP00000407922.2:n.194-20_194-19insTGT
ENST00000502666.1:c.399-20_399-19insTGT ENSP00000461951.1:n.399-20_399-19insTGT
ENST00000507596.5:c.194-20_194-19insTGT ENSP00000424291.1:n.194-20_194-19insTGT
ENST00000508384.5:c.-239-20_-239-19insTGT ENSP00000464289.1:n.-239-20_-239-19insTGT
ENST00000510434.1:c.194-20_194-19insTGT ENSP00000423051.1:n.194-20_194-19insTGT
ENST00000514502.1:c.*211-20_*211-19insTGT ENSP00000425924.1:n.*211-20_*211-19insTGT
ENST00000515760.1:n.328-20_328-19insTGT
NM_002617.3:c.194-20_194-19insTGT NP_002608.1:n.194-20_194-19insTGT
NM_153818.1:c.194-20_194-19insTGT NP_722540.1:n.194-20_194-19insTGT
XM_011541573.1:c.194-20_194-19insTGT XP_011539875.1:n.194-20_194-19insTGT
XM_011541574.1:c.-239-20_-239-19insTGT XP_011539876.1:n.-239-20_-239-19insTGT
XM_011541575.1:c.-239-20_-239-19insTGT XP_011539877.1:n.-239-20_-239-19insTGT
XM_011541576.1:c.194-20_194-19insTGT XP_011539878.1:n.194-20_194-19insTGT
XR_946666.1:n.314-20_314-19insTGT
XM_011541576.2:c.194-20_194-19insTGT XP_011539878.1:n.194-20_194-19insTGT
XR_946666.2:n.263-20_263-19insTGT
NM_001374425.1:c.194-20_194-19insTGT NP_001361354.1:n.194-20_194-19insTGT
NM_001374426.1:c.-239-20_-239-19insTGT NP_001361355.1:n.-239-20_-239-19insTGT
NM_001374427.1:c.-239-20_-239-19insTGT NP_001361356.1:n.-239-20_-239-19insTGT
NM_002617.4:c.194-20_194-19insTGT MANE Select NP_002608.1:n.194-20_194-19insTGT
NM_153818.2:c.194-20_194-19insTGT NP_722540.1:n.194-20_194-19insTGT
NR_164636.1:n.313-20_313-19insTGT