Canonical Allele Identifier: CA1153259925

Gene: PEX14

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10506158A>C , CM000663.2:g.10506158A>C	GRCh38
NC_000001.10:g.10566215A>C , CM000663.1:g.10566215A>C	GRCh37
NC_000001.9:g.10488802A>C	NCBI36
NG_008340.1:g.36213A>C
NG_008340.2:g.36213A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356607.9:c.84+10837A>C MANE Select	ENSP00000349016.4:n.84+10837A>C
ENST00000356607.8:c.84+10837A>C	ENSP00000349016.4:n.84+10837A>C
ENST00000472851.1:n.341+10837A>C
ENST00000491661.2:c.69+10837A>C	ENSP00000465473.1:n.69+10837A>C
NM_004565.2:c.84+10837A>C	NP_004556.1:n.84+10837A>C
XM_011541577.1:c.126+10837A>C	XP_011539879.1:n.126+10837A>C
XM_011541579.1:c.126+10837A>C	XP_011539881.1:n.126+10837A>C
XM_011541580.1:c.84+10837A>C	XP_011539882.1:n.84+10837A>C
XM_011541577.2:c.126+10837A>C	XP_011539879.1:n.126+10837A>C
XM_011541579.3:c.126+10837A>C	XP_011539881.1:n.126+10837A>C
XM_024447651.1:c.-109+10837A>C	XP_024303419.1:n.-109+10837A>C
NM_004565.3:c.84+10837A>C MANE Select	NP_004556.1:n.84+10837A>C