Canonical Allele Identifier: CA337984226

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2337960A>G (hg19) ; chr1:g.2406521A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406521A>G , CM000663.2:g.2406521A>G	GRCh38
NC_000001.10:g.2337960A>G , CM000663.1:g.2337960A>G	GRCh37
NC_000001.9:g.2327820A>G	NCBI36
NG_008342.1:g.11051T>C
NG_016128.1:g.19747A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.935T>C	ENSP00000288774.3:p.Phe312Ser
ENST00000447513.7:c.875T>C MANE Select	ENSP00000407922.2:p.Phe292Ser
ENST00000650293.1:c.829T>C
ENST00000288774.7:c.935T>C	ENSP00000288774.3:p.Phe312Ser
ENST00000447513.6:c.875T>C	ENSP00000407922.2:p.Phe292Ser
ENST00000507596.5:c.875T>C	ENSP00000424291.1:p.Phe292Ser
ENST00000510434.1:c.*241T>C	ENSP00000423051.1:n.*241T>C
NM_002617.3:c.875T>C	NP_002608.1:p.Phe292Ser
NM_153818.1:c.935T>C	NP_722540.1:p.Phe312Ser
XM_011541573.1:c.932T>C	XP_011539875.1:p.Phe311Ser
XM_011541574.1:c.500T>C	XP_011539876.1:p.Phe167Ser
XM_011541575.1:c.500T>C	XP_011539877.1:p.Phe167Ser
XR_946666.1:n.991T>C
XR_946666.2:n.940T>C
NM_001374425.1:c.932T>C	NP_001361354.1:p.Phe311Ser
NM_001374426.1:c.500T>C	NP_001361355.1:p.Phe167Ser
NM_001374427.1:c.443T>C	NP_001361356.1:p.Phe148Ser
NM_002617.4:c.875T>C MANE Select	NP_002608.1:p.Phe292Ser
NM_153818.2:c.935T>C	NP_722540.1:p.Phe312Ser
NR_164636.1:n.990T>C