Canonical Allele Identifier: CA364155641

Gene: PEX6

Linked Data

• MyVariant Identifiers: chr6:g.42937441T>G (hg19) ; chr6:g.42969703T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42969703T>G , CM000668.2:g.42969703T>G	GRCh38
NC_000006.11:g.42937441T>G , CM000668.1:g.42937441T>G	GRCh37
NC_000006.10:g.43045419T>G	NCBI36
NG_008370.1:g.14541A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304611.13:c.1332A>C MANE Select	ENSP00000303511.8:p.Glu444Asp
ENST00000244546.4:c.1332A>C	ENSP00000244546.4:p.Glu444Asp
ENST00000304611.12:c.1332A>C	ENSP00000303511.8:p.Glu444Asp
NM_000287.3:c.1332A>C	NP_000278.3:p.Glu444Asp
NM_001316313.1:c.1068A>C	NP_001303242.1:p.Glu356Asp
NR_133009.1:n.1425A>C
XM_011514661.1:c.1248A>C	XP_011512963.1:p.Glu416Asp
XR_926246.1:n.1425A>C
XM_011514661.2:c.1248A>C	XP_011512963.1:p.Glu416Asp
XR_001743466.2:n.2406A>C
NM_000287.4:c.1332A>C MANE Select	NP_000278.3:p.Glu444Asp
NM_001316313.2:c.1068A>C	NP_001303242.1:p.Glu356Asp
NR_133009.2:n.1363A>C