Canonical Allele Identifier: CA1140422510

Gene: PEX14

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10578547C= , CM000663.2:g.10578547C=	GRCh38
NC_000001.10:g.10638604C= , CM000663.1:g.10638604C=	GRCh37
NC_000001.9:g.10561191C=	NCBI36
NG_008340.1:g.108602C=
NG_008340.2:g.108602C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356607.9:c.170-20691C= MANE Select	ENSP00000349016.4:n.170-20691C=
ENST00000356607.8:c.170-20691C=	ENSP00000349016.4:n.170-20691C=
ENST00000491661.2:c.155-20691C=	ENSP00000465473.1:n.155-20691C=
NM_004565.2:c.170-20691C=	NP_004556.1:n.170-20691C=
XM_005263470.3:c.-23-20691C=	XP_005263527.1:n.-23-20691C=
XM_011541577.1:c.212-20691C=	XP_011539879.1:n.212-20691C=
XM_011541578.1:c.113-20691C=	XP_011539880.1:n.113-20691C=
XM_011541579.1:c.212-39785C=	XP_011539881.1:n.212-39785C=
XM_011541580.1:c.170-39785C=	XP_011539882.1:n.170-39785C=
XM_005263470.5:c.-23-20691C=	XP_005263527.1:n.-23-20691C=
XM_011541577.2:c.212-20691C=	XP_011539879.1:n.212-20691C=
XM_011541578.2:c.113-20691C=	XP_011539880.1:n.113-20691C=
XM_011541579.3:c.212-39785C=	XP_011539881.1:n.212-39785C=
XM_024447651.1:c.-23-20691C=	XP_024303419.1:n.-23-20691C=
NM_004565.3:c.170-20691C= MANE Select	NP_004556.1:n.170-20691C=