Canonical Allele Identifier: CA337984141

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2337947G>C (hg19) ; chr1:g.2406508G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406508G>C , CM000663.2:g.2406508G>C	GRCh38
NC_000001.10:g.2337947G>C , CM000663.1:g.2337947G>C	GRCh37
NC_000001.9:g.2327807G>C	NCBI36
NG_008342.1:g.11064C>G
NG_016128.1:g.19734G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.948C>G	ENSP00000288774.3:p.Cys316Trp
ENST00000447513.7:c.888C>G MANE Select	ENSP00000407922.2:p.Cys296Trp
ENST00000650293.1:c.842C>G
ENST00000288774.7:c.948C>G	ENSP00000288774.3:p.Cys316Trp
ENST00000447513.6:c.888C>G	ENSP00000407922.2:p.Cys296Trp
ENST00000507596.5:c.888C>G	ENSP00000424291.1:p.Cys296Trp
NM_002617.3:c.888C>G	NP_002608.1:p.Cys296Trp
NM_153818.1:c.948C>G	NP_722540.1:p.Cys316Trp
XM_011541573.1:c.945C>G	XP_011539875.1:p.Cys315Trp
XM_011541574.1:c.513C>G	XP_011539876.1:p.Cys171Trp
XM_011541575.1:c.513C>G	XP_011539877.1:p.Cys171Trp
XR_946666.1:n.1004C>G
XR_946666.2:n.953C>G
NM_001374425.1:c.945C>G	NP_001361354.1:p.Cys315Trp
NM_001374426.1:c.513C>G	NP_001361355.1:p.Cys171Trp
NM_001374427.1:c.456C>G	NP_001361356.1:p.Cys152Trp
NM_002617.4:c.888C>G MANE Select	NP_002608.1:p.Cys296Trp
NM_153818.2:c.948C>G	NP_722540.1:p.Cys316Trp
NR_164636.1:n.1003C>G