Canonical Allele Identifier: CA450366122

Gene: PEX6

Linked Data

• ClinVar Variation Id: 2717327
• ClinVar RCV Id: RCV003530703
• gnomAD v4: 6-42969799-C-A
• MyVariant Identifiers: chr6:g.42937537C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42969799C>A , CM000668.2:g.42969799C>A	GRCh38
NC_000006.11:g.42937537C>A , CM000668.1:g.42937537C>A	GRCh37
NC_000006.10:g.43045515C>A	NCBI36
NG_008370.1:g.14445G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304611.13:c.1236G>T MANE Select	ENSP00000303511.8:p.Val412=
ENST00000244546.4:c.1236G>T	ENSP00000244546.4:p.Val412=
ENST00000304611.12:c.1236G>T	ENSP00000303511.8:p.Val412=
NM_000287.3:c.1236G>T	NP_000278.3:p.Val412=
NM_001316313.1:c.972G>T	NP_001303242.1:p.Val324=
NR_133009.1:n.1329G>T
XM_011514661.1:c.1152G>T	XP_011512963.1:p.Val384=
XR_926246.1:n.1329G>T
XM_011514661.2:c.1152G>T	XP_011512963.1:p.Val384=
XR_001743466.2:n.2310G>T
NM_000287.4:c.1236G>T MANE Select	NP_000278.3:p.Val412=
NM_001316313.2:c.972G>T	NP_001303242.1:p.Val324=
NR_133009.2:n.1267G>T