Canonical Allele Identifier: CA138238795
Community Standard Title: NM_000287.4(PEX6):c.35T>C (p.Phe12Ser)
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42979116A>G , CM000668.2:g.42979116A>G GRCh38
NC_000006.11:g.42946854A>G , CM000668.1:g.42946854A>G GRCh37
NC_000006.10:g.43054832A>G NCBI36
NG_008370.1:g.5128T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000287.4:c.35T>C MANE Select NP_000278.3:p.Phe12Ser
ENST00000304611.13:c.35T>C MANE Select ENSP00000303511.8:p.Phe12Ser
NM_000287.3:c.35T>C NP_000278.3:p.Phe12Ser
NM_001316313.1:c.35T>C NP_001303242.1:p.Phe12Ser
NM_001316313.2:c.35T>C NP_001303242.1:p.Phe12Ser
NR_133009.1:n.128T>C
NR_133009.2:n.66T>C
ENST00000244546.4:c.35T>C ENSP00000244546.4:p.Phe12Ser
ENST00000304611.12:c.35T>C ENSP00000303511.8:p.Phe12Ser
XM_011514661.1:c.35T>C XP_011512963.1:p.Phe12Ser
XM_011514661.2:c.35T>C XP_011512963.1:p.Phe12Ser
XR_001743466.2:n.1109T>C
XR_926246.1:n.128T>C