Canonical Allele Identifier: CA337984273

Gene: PEX10

Linked Data

• MyVariant Identifiers: chr1:g.2337969C>A (hg19) ; chr1:g.2406530C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406530C>A , CM000663.2:g.2406530C>A	GRCh38
NC_000001.10:g.2337969C>A , CM000663.1:g.2337969C>A	GRCh37
NC_000001.9:g.2327829C>A	NCBI36
NG_008342.1:g.11042G>T
NG_016128.1:g.19756C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.926G>T	ENSP00000288774.3:p.Gly309Val
ENST00000447513.7:c.866G>T MANE Select	ENSP00000407922.2:p.Gly289Val
ENST00000650293.1:c.820G>T
ENST00000288774.7:c.926G>T	ENSP00000288774.3:p.Gly309Val
ENST00000447513.6:c.866G>T	ENSP00000407922.2:p.Gly289Val
ENST00000507596.5:c.866G>T	ENSP00000424291.1:p.Gly289Val
ENST00000510434.1:c.*232G>T	ENSP00000423051.1:n.*232G>T
NM_002617.3:c.866G>T	NP_002608.1:p.Gly289Val
NM_153818.1:c.926G>T	NP_722540.1:p.Gly309Val
XM_011541573.1:c.923G>T	XP_011539875.1:p.Gly308Val
XM_011541574.1:c.491G>T	XP_011539876.1:p.Gly164Val
XM_011541575.1:c.491G>T	XP_011539877.1:p.Gly164Val
XR_946666.1:n.982G>T
XR_946666.2:n.931G>T
NM_001374425.1:c.923G>T	NP_001361354.1:p.Gly308Val
NM_001374426.1:c.491G>T	NP_001361355.1:p.Gly164Val
NM_001374427.1:c.434G>T	NP_001361356.1:p.Gly145Val
NM_002617.4:c.866G>T MANE Select	NP_002608.1:p.Gly289Val
NM_153818.2:c.926G>T	NP_722540.1:p.Gly309Val
NR_164636.1:n.981G>T