Canonical Allele Identifier: CA364155782

Gene: PEX6

Linked Data

• MyVariant Identifiers: chr6:g.42937485A>C (hg19) ; chr6:g.42969747A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42969747A>C , CM000668.2:g.42969747A>C	GRCh38
NC_000006.11:g.42937485A>C , CM000668.1:g.42937485A>C	GRCh37
NC_000006.10:g.43045463A>C	NCBI36
NG_008370.1:g.14497T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304611.13:c.1288T>G MANE Select	ENSP00000303511.8:p.Trp430Gly
ENST00000244546.4:c.1288T>G	ENSP00000244546.4:p.Trp430Gly
ENST00000304611.12:c.1288T>G	ENSP00000303511.8:p.Trp430Gly
NM_000287.3:c.1288T>G	NP_000278.3:p.Trp430Gly
NM_001316313.1:c.1024T>G	NP_001303242.1:p.Trp342Gly
NR_133009.1:n.1381T>G
XM_011514661.1:c.1204T>G	XP_011512963.1:p.Trp402Gly
XR_926246.1:n.1381T>G
XM_011514661.2:c.1204T>G	XP_011512963.1:p.Trp402Gly
XR_001743466.2:n.2362T>G
NM_000287.4:c.1288T>G MANE Select	NP_000278.3:p.Trp430Gly
NM_001316313.2:c.1024T>G	NP_001303242.1:p.Trp342Gly
NR_133009.2:n.1319T>G