Canonical Allele Identifier: CA337988637

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2340177A>G (hg19) ; chr1:g.2408738A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408738A>G , CM000663.2:g.2408738A>G	GRCh38
NC_000001.10:g.2340177A>G , CM000663.1:g.2340177A>G	GRCh37
NC_000001.9:g.2330037A>G	NCBI36
NG_008342.1:g.8834T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.314T>C	ENSP00000288774.3:p.Leu105Pro
ENST00000447513.7:c.314T>C MANE Select	ENSP00000407922.2:p.Leu105Pro
ENST00000650293.1:c.268T>C
ENST00000288774.7:c.314T>C	ENSP00000288774.3:p.Leu105Pro
ENST00000447513.6:c.314T>C	ENSP00000407922.2:p.Leu105Pro
ENST00000502666.1:c.519T>C	ENSP00000461951.1:n.519T>C
ENST00000507596.5:c.314T>C	ENSP00000424291.1:p.Leu105Pro
ENST00000508384.5:c.-119T>C	ENSP00000464289.1:n.-119T>C
ENST00000510434.1:c.314T>C	ENSP00000423051.1:p.Leu105Pro
ENST00000515760.1:n.448T>C
NM_002617.3:c.314T>C	NP_002608.1:p.Leu105Pro
NM_153818.1:c.314T>C	NP_722540.1:p.Leu105Pro
XM_011541573.1:c.314T>C	XP_011539875.1:p.Leu105Pro
XM_011541574.1:c.-119T>C	XP_011539876.1:n.-119T>C
XM_011541575.1:c.-119T>C	XP_011539877.1:n.-119T>C
XM_011541576.1:c.314T>C	XP_011539878.1:p.Leu105Pro
XR_946666.1:n.434T>C
XM_011541576.2:c.314T>C	XP_011539878.1:p.Leu105Pro
XR_946666.2:n.383T>C
NM_001374425.1:c.314T>C	NP_001361354.1:p.Leu105Pro
NM_001374426.1:c.-119T>C	NP_001361355.1:n.-119T>C
NM_001374427.1:c.-119T>C	NP_001361356.1:n.-119T>C
NM_002617.4:c.314T>C MANE Select	NP_002608.1:p.Leu105Pro
NM_153818.2:c.314T>C	NP_722540.1:p.Leu105Pro
NR_164636.1:n.433T>C