Canonical Allele Identifier: CA364155664

Gene: PEX6

Linked Data

• dbSNP Id: rs1769990462
• gnomAD v3: 6-42969713-A-G
• gnomAD v4: 6-42969713-A-G
• MyVariant Identifiers: chr6:g.42937451A>G (hg19) ; chr6:g.42969713A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42969713A>G , CM000668.2:g.42969713A>G	GRCh38
NC_000006.11:g.42937451A>G , CM000668.1:g.42937451A>G	GRCh37
NC_000006.10:g.43045429A>G	NCBI36
NG_008370.1:g.14531T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304611.13:c.1322T>C MANE Select	ENSP00000303511.8:p.Leu441Ser
ENST00000244546.4:c.1322T>C	ENSP00000244546.4:p.Leu441Ser
ENST00000304611.12:c.1322T>C	ENSP00000303511.8:p.Leu441Ser
NM_000287.3:c.1322T>C	NP_000278.3:p.Leu441Ser
NM_001316313.1:c.1058T>C	NP_001303242.1:p.Leu353Ser
NR_133009.1:n.1415T>C
XM_011514661.1:c.1238T>C	XP_011512963.1:p.Leu413Ser
XR_926246.1:n.1415T>C
XM_011514661.2:c.1238T>C	XP_011512963.1:p.Leu413Ser
XR_001743466.2:n.2396T>C
NM_000287.4:c.1322T>C MANE Select	NP_000278.3:p.Leu441Ser
NM_001316313.2:c.1058T>C	NP_001303242.1:p.Leu353Ser
NR_133009.2:n.1353T>C