Canonical Allele Identifier: CA399136828
Gene: PEX12 HGNC NCBI

Linked Data

dbSNP Id: rs2072781122

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35575817G>C , CM000679.2:g.35575817G>C GRCh38
NC_000017.10:g.33902836G>C , CM000679.1:g.33902836G>C GRCh37
NC_000017.9:g.30926949G>C NCBI36
NG_008447.1:g.7821C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000225873.9:c.1045C>G MANE Select ENSP00000225873.3:p.Gln349Glu
ENST00000586663.2:c.1045C>G ENSP00000466894.2:p.Gln349Glu
ENST00000225873.8:c.1045C>G ENSP00000225873.3:p.Gln349Glu
ENST00000586663.1:c.1045C>G ENSP00000466894.1:p.Gln349Glu
ENST00000613219.4:c.1045C>G ENSP00000482609.1:p.Gln349Glu
NM_000286.2:c.1045C>G NP_000277.1:p.Gln349Glu
NM_000286.3:c.1045C>G MANE Select NP_000277.1:p.Gln349Glu