Canonical Allele Identifier: CA3811569
Community Standard Title: NM_000287.4(PEX6):c.759T>C (p.Asp253=)
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42978392A>G , CM000668.2:g.42978392A>G GRCh38
NC_000006.11:g.42946130A>G , CM000668.1:g.42946130A>G GRCh37
NC_000006.10:g.43054108A>G NCBI36
NG_008370.1:g.5852T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000287.4:c.759T>C MANE Select NP_000278.3:p.Asp253=
ENST00000304611.13:c.759T>C MANE Select ENSP00000303511.8:p.Asp253=
NM_000287.3:c.759T>C NP_000278.3:p.Asp253=
NM_001316313.1:c.618+141T>C NP_001303242.1:n.618+141T>C
NM_001316313.2:c.618+141T>C NP_001303242.1:n.618+141T>C
NR_133009.1:n.852T>C
NR_133009.2:n.790T>C
ENST00000244546.4:c.759T>C ENSP00000244546.4:p.Asp253=
ENST00000304611.12:c.759T>C ENSP00000303511.8:p.Asp253=
XM_011514661.1:c.759T>C XP_011512963.1:p.Asp253=
XM_011514661.2:c.759T>C XP_011512963.1:p.Asp253=
XR_001743466.2:n.1833T>C
XR_926246.1:n.852T>C