Canonical Allele Identifier: CA365766569

Gene: PEX7

Linked Data

• gnomAD v4: 6-136898161-C-A
• MyVariant Identifiers: chr6:g.137219299C>A (hg19) ; chr6:g.136898161C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136898161C>A , CM000668.2:g.136898161C>A	GRCh38
NC_000006.11:g.137219299C>A , CM000668.1:g.137219299C>A	GRCh37
NC_000006.10:g.137260992C>A	NCBI36
NG_008462.1:g.80582C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.823C>A MANE Select	ENSP00000315680.3:p.Pro275Thr
ENST00000541292.6:c.*88C>A	ENSP00000441004.1:n.*88C>A
ENST00000678002.1:c.511C>A
ENST00000678557.1:c.709C>A	ENSP00000502962.1:p.Pro237Thr
ENST00000679286.1:c.703C>A	ENSP00000503168.1:p.Pro235Thr
ENST00000318471.4:c.823C>A	ENSP00000315680.3:p.Pro275Thr
NM_000288.3:c.823C>A	NP_000279.1:p.Pro275Thr
XM_005267019.3:c.709C>A	XP_005267076.1:p.Pro237Thr
XM_006715502.1:c.529C>A	XP_006715565.1:p.Pro177Thr
XM_011535900.1:c.546C>A	XP_011534202.1:p.Ser182Arg
XM_005267019.4:c.709C>A	XP_005267076.1:p.Pro237Thr
XM_006715502.2:c.529C>A	XP_006715565.1:p.Pro177Thr
XM_017010934.2:c.546C>A	XP_016866423.1:p.Ser182Arg
NM_000288.4:c.823C>A MANE Select	NP_000279.1:p.Pro275Thr