Canonical Allele Identifier: CA364155949

Gene: PEX6

Linked Data

• MyVariant Identifiers: chr6:g.42937535C>G (hg19) ; chr6:g.42969797C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42969797C>G , CM000668.2:g.42969797C>G	GRCh38
NC_000006.11:g.42937535C>G , CM000668.1:g.42937535C>G	GRCh37
NC_000006.10:g.43045513C>G	NCBI36
NG_008370.1:g.14447G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304611.13:c.1238G>C MANE Select	ENSP00000303511.8:p.Gly413Ala
ENST00000244546.4:c.1238G>C	ENSP00000244546.4:p.Gly413Ala
ENST00000304611.12:c.1238G>C	ENSP00000303511.8:p.Gly413Ala
NM_000287.3:c.1238G>C	NP_000278.3:p.Gly413Ala
NM_001316313.1:c.974G>C	NP_001303242.1:p.Gly325Ala
NR_133009.1:n.1331G>C
XM_011514661.1:c.1154G>C	XP_011512963.1:p.Gly385Ala
XR_926246.1:n.1331G>C
XM_011514661.2:c.1154G>C	XP_011512963.1:p.Gly385Ala
XR_001743466.2:n.2312G>C
NM_000287.4:c.1238G>C MANE Select	NP_000278.3:p.Gly413Ala
NM_001316313.2:c.974G>C	NP_001303242.1:p.Gly325Ala
NR_133009.2:n.1269G>C