Canonical Allele Identifier: CA450366014

Gene: PEX6

Linked Data

• MyVariant Identifiers: chr6:g.42937465T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42969727T>C , CM000668.2:g.42969727T>C	GRCh38
NC_000006.11:g.42937465T>C , CM000668.1:g.42937465T>C	GRCh37
NC_000006.10:g.43045443T>C	NCBI36
NG_008370.1:g.14517A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000304611.13:c.1308A>G MANE Select	ENSP00000303511.8:p.Pro436=
ENST00000244546.4:c.1308A>G	ENSP00000244546.4:p.Pro436=
ENST00000304611.12:c.1308A>G	ENSP00000303511.8:p.Pro436=
NM_000287.3:c.1308A>G	NP_000278.3:p.Pro436=
NM_001316313.1:c.1044A>G	NP_001303242.1:p.Pro348=
NR_133009.1:n.1401A>G
XM_011514661.1:c.1224A>G	XP_011512963.1:p.Pro408=
XR_926246.1:n.1401A>G
XM_011514661.2:c.1224A>G	XP_011512963.1:p.Pro408=
XR_001743466.2:n.2382A>G
NM_000287.4:c.1308A>G MANE Select	NP_000278.3:p.Pro436=
NM_001316313.2:c.1044A>G	NP_001303242.1:p.Pro348=
NR_133009.2:n.1339A>G