Canonical Allele Identifier: CA337984213

Gene: PEX10

Linked Data

• gnomAD v4: 1-2406520-G-T
• MyVariant Identifiers: chr1:g.2337959G>T (hg19) ; chr1:g.2406520G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406520G>T , CM000663.2:g.2406520G>T	GRCh38
NC_000001.10:g.2337959G>T , CM000663.1:g.2337959G>T	GRCh37
NC_000001.9:g.2327819G>T	NCBI36
NG_008342.1:g.11052C>A
NG_016128.1:g.19746G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.936C>A	ENSP00000288774.3:p.Phe312Leu
ENST00000447513.7:c.876C>A MANE Select	ENSP00000407922.2:p.Phe292Leu
ENST00000650293.1:c.830C>A
ENST00000288774.7:c.936C>A	ENSP00000288774.3:p.Phe312Leu
ENST00000447513.6:c.876C>A	ENSP00000407922.2:p.Phe292Leu
ENST00000507596.5:c.876C>A	ENSP00000424291.1:p.Phe292Leu
ENST00000510434.1:c.*242C>A	ENSP00000423051.1:n.*242C>A
NM_002617.3:c.876C>A	NP_002608.1:p.Phe292Leu
NM_153818.1:c.936C>A	NP_722540.1:p.Phe312Leu
XM_011541573.1:c.933C>A	XP_011539875.1:p.Phe311Leu
XM_011541574.1:c.501C>A	XP_011539876.1:p.Phe167Leu
XM_011541575.1:c.501C>A	XP_011539877.1:p.Phe167Leu
XR_946666.1:n.992C>A
XR_946666.2:n.941C>A
NM_001374425.1:c.933C>A	NP_001361354.1:p.Phe311Leu
NM_001374426.1:c.501C>A	NP_001361355.1:p.Phe167Leu
NM_001374427.1:c.444C>A	NP_001361356.1:p.Phe148Leu
NM_002617.4:c.876C>A MANE Select	NP_002608.1:p.Phe292Leu
NM_153818.2:c.936C>A	NP_722540.1:p.Phe312Leu
NR_164636.1:n.991C>A