Canonical Allele Identifier: CA2742186693
Gene: PEX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2408874_2408875insAGA , CM000663.2:g.2408874_2408875insAGA GRCh38
NC_000001.10:g.2340313_2340314insAGA , CM000663.1:g.2340313_2340314insAGA GRCh37
NC_000001.9:g.2330173_2330174insAGA NCBI36
NG_008342.1:g.8697_8698insTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000288774.8:c.194-17_194-16insTCT ENSP00000288774.3:n.194-17_194-16insTCT
ENST00000447513.7:c.194-17_194-16insTCT MANE Select ENSP00000407922.2:n.194-17_194-16insTCT
ENST00000650293.1:c.148-17_148-16insTCT
ENST00000288774.7:c.194-17_194-16insTCT ENSP00000288774.3:n.194-17_194-16insTCT
ENST00000447513.6:c.194-17_194-16insTCT ENSP00000407922.2:n.194-17_194-16insTCT
ENST00000502666.1:c.399-17_399-16insTCT ENSP00000461951.1:n.399-17_399-16insTCT
ENST00000507596.5:c.194-17_194-16insTCT ENSP00000424291.1:n.194-17_194-16insTCT
ENST00000508384.5:c.-239-17_-239-16insTCT ENSP00000464289.1:n.-239-17_-239-16insTCT
ENST00000510434.1:c.194-17_194-16insTCT ENSP00000423051.1:n.194-17_194-16insTCT
ENST00000514502.1:c.*211-17_*211-16insTCT ENSP00000425924.1:n.*211-17_*211-16insTCT
ENST00000515760.1:n.328-17_328-16insTCT
NM_002617.3:c.194-17_194-16insTCT NP_002608.1:n.194-17_194-16insTCT
NM_153818.1:c.194-17_194-16insTCT NP_722540.1:n.194-17_194-16insTCT
XM_011541573.1:c.194-17_194-16insTCT XP_011539875.1:n.194-17_194-16insTCT
XM_011541574.1:c.-239-17_-239-16insTCT XP_011539876.1:n.-239-17_-239-16insTCT
XM_011541575.1:c.-239-17_-239-16insTCT XP_011539877.1:n.-239-17_-239-16insTCT
XM_011541576.1:c.194-17_194-16insTCT XP_011539878.1:n.194-17_194-16insTCT
XR_946666.1:n.314-17_314-16insTCT
XM_011541576.2:c.194-17_194-16insTCT XP_011539878.1:n.194-17_194-16insTCT
XR_946666.2:n.263-17_263-16insTCT
NM_001374425.1:c.194-17_194-16insTCT NP_001361354.1:n.194-17_194-16insTCT
NM_001374426.1:c.-239-17_-239-16insTCT NP_001361355.1:n.-239-17_-239-16insTCT
NM_001374427.1:c.-239-17_-239-16insTCT NP_001361356.1:n.-239-17_-239-16insTCT
NM_002617.4:c.194-17_194-16insTCT MANE Select NP_002608.1:n.194-17_194-16insTCT
NM_153818.2:c.194-17_194-16insTCT NP_722540.1:n.194-17_194-16insTCT
NR_164636.1:n.313-17_313-16insTCT