Canonical Allele Identifier: CA4341276

Gene: PEX1

Linked Data

• dbSNP Id: rs376600394
• ExAC: 7:92135590 C / T
• gnomAD v2: 7-92135590-C-T
• MyVariant Identifiers: chr7:g.92135590C>T (hg19) ; chr7:g.92506276C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92506276C>T , CM000669.2:g.92506276C>T	GRCh38
NC_000007.13:g.92135590C>T , CM000669.1:g.92135590C>T	GRCh37
NC_000007.12:g.91973526C>T	NCBI36
NG_008341.1:g.27256G>A
NG_008341.2:g.27256G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1872G>A MANE Select	ENSP00000248633.4:p.Val624=
ENST00000248633.8:c.1872G>A	ENSP00000248633.4:p.Val624=
ENST00000422866.1:c.690G>A
ENST00000428214.5:c.1872G>A	ENSP00000394413.1:p.Val624=
ENST00000438045.5:c.906G>A	ENSP00000410438.1:p.Val302=
ENST00000484913.5:n.1911G>A
ENST00000496420.5:n.1548G>A
NM_000466.2:c.1872G>A	NP_000457.1:p.Val624=
NM_001282677.1:c.1872G>A	NP_001269606.1:p.Val624=
NM_001282678.1:c.1248G>A	NP_001269607.1:p.Val416=
XM_005250433.3:c.123G>A	XP_005250490.1:p.Val41=
XR_242246.3:n.1968G>A
XM_017012319.2:c.123G>A	XP_016867808.1:p.Val41=
XR_001744808.2:n.899G>A
XR_242246.5:n.1919G>A
NM_000466.3:c.1872G>A MANE Select	NP_000457.1:p.Val624=
NM_001282677.2:c.1872G>A	NP_001269606.1:p.Val624=
NM_001282678.2:c.1248G>A	NP_001269607.1:p.Val416=