Canonical Allele Identifier: CA512912649

Gene: PEX26

Linked Data

• MyVariant Identifiers: chr22:g.18560966T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18078200T>C , CM000684.2:g.18078200T>C	GRCh38
NC_000022.10:g.18560966T>C , CM000684.1:g.18560966T>C	GRCh37
NC_000022.9:g.16940966T>C	NCBI36
NG_008339.1:g.5281T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.-177T>C MANE Select	ENSP00000382648.4:n.-177T>C
ENST00000474897.6:c.-81-96T>C	ENSP00000434235.2:n.-81-96T>C
ENST00000329627.11:c.-81-96T>C	ENSP00000331106.5:n.-81-96T>C
ENST00000399744.7:c.-177T>C	ENSP00000382648.3:n.-177T>C
ENST00000474897.5:c.-177T>C	ENSP00000434235.1:n.-177T>C
ENST00000610387.4:c.-81-96T>C	ENSP00000482091.1:n.-81-96T>C
NM_001127649.2:c.-177T>C	NP_001121121.1:n.-177T>C
NM_001199319.1:c.-81-96T>C	NP_001186248.1:n.-81-96T>C
NM_017929.5:c.-81-96T>C	NP_060399.1:n.-81-96T>C
NM_001127649.3:c.-177T>C MANE Select	NP_001121121.1:n.-177T>C
NM_001199319.2:c.-81-96T>C	NP_001186248.1:n.-81-96T>C
NM_017929.6:c.-81-96T>C	NP_060399.1:n.-81-96T>C