Canonical Allele Identifier: CA1140725586

Gene: PEX14

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10624405C= , CM000663.2:g.10624405C=	GRCh38
NC_000001.10:g.10684462C= , CM000663.1:g.10684462C=	GRCh37
NC_000001.9:g.10607049C=	NCBI36
NG_008340.1:g.154460C=
NG_008340.2:g.154460C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356607.9:c.553C= MANE Select	ENSP00000349016.4:p.Gln185=
ENST00000356607.8:c.553C=	ENSP00000349016.4:p.Gln185=
NM_004565.2:c.553C=	NP_004556.1:p.Gln185=
XM_005263470.3:c.361C=	XP_005263527.1:p.Gln121=
XM_011541577.1:c.595C=	XP_011539879.1:p.Gln199=
XM_011541578.1:c.496C=	XP_011539880.1:p.Gln166=
XM_011541579.1:c.466C=	XP_011539881.1:p.Gln156=
XM_011541580.1:c.424C=	XP_011539882.1:p.Gln142=
XM_005263470.5:c.361C=	XP_005263527.1:p.Gln121=
XM_011541577.2:c.595C=	XP_011539879.1:p.Gln199=
XM_011541578.2:c.496C=	XP_011539880.1:p.Gln166=
XM_011541579.3:c.466C=	XP_011539881.1:p.Gln156=
XM_024447651.1:c.361C=	XP_024303419.1:p.Gln121=
NM_004565.3:c.553C= MANE Select	NP_004556.1:p.Gln185=