Canonical Allele Identifier: CA364155670

Gene: PEX6

Linked Data

• MyVariant Identifiers: chr6:g.42937454G>A (hg19) ; chr6:g.42969716G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42969716G>A , CM000668.2:g.42969716G>A	GRCh38
NC_000006.11:g.42937454G>A , CM000668.1:g.42937454G>A	GRCh37
NC_000006.10:g.43045432G>A	NCBI36
NG_008370.1:g.14528C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304611.13:c.1319C>T MANE Select	ENSP00000303511.8:p.Ala440Val
ENST00000244546.4:c.1319C>T	ENSP00000244546.4:p.Ala440Val
ENST00000304611.12:c.1319C>T	ENSP00000303511.8:p.Ala440Val
NM_000287.3:c.1319C>T	NP_000278.3:p.Ala440Val
NM_001316313.1:c.1055C>T	NP_001303242.1:p.Ala352Val
NR_133009.1:n.1412C>T
XM_011514661.1:c.1235C>T	XP_011512963.1:p.Ala412Val
XR_926246.1:n.1412C>T
XM_011514661.2:c.1235C>T	XP_011512963.1:p.Ala412Val
XR_001743466.2:n.2393C>T
NM_000287.4:c.1319C>T MANE Select	NP_000278.3:p.Ala440Val
NM_001316313.2:c.1055C>T	NP_001303242.1:p.Ala352Val
NR_133009.2:n.1350C>T