Canonical Allele Identifier: CA368174226

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92129137C>G (hg19) ; chr7:g.92499823C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92499823C>G , CM000669.2:g.92499823C>G	GRCh38
NC_000007.13:g.92129137C>G , CM000669.1:g.92129137C>G	GRCh37
NC_000007.12:g.91967073C>G	NCBI36
NG_008341.1:g.33709G>C
NG_008341.2:g.33709G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2599G>C MANE Select	ENSP00000248633.4:p.Ala867Pro
ENST00000248633.8:c.2599G>C	ENSP00000248633.4:p.Ala867Pro
ENST00000428214.5:c.2428G>C	ENSP00000394413.1:p.Ala810Pro
ENST00000438045.5:c.1633G>C	ENSP00000410438.1:p.Ala545Pro
ENST00000484913.5:n.2638G>C
ENST00000496420.5:n.2491G>C
NM_000466.2:c.2599G>C	NP_000457.1:p.Ala867Pro
NM_001282677.1:c.2428G>C	NP_001269606.1:p.Ala810Pro
NM_001282678.1:c.1975G>C	NP_001269607.1:p.Ala659Pro
XM_005250433.3:c.850G>C	XP_005250490.1:p.Ala284Pro
XR_242246.3:n.2695G>C
XM_017012319.2:c.850G>C	XP_016867808.1:p.Ala284Pro
XR_001744808.2:n.1626G>C
XR_242246.5:n.2646G>C
NM_000466.3:c.2599G>C MANE Select	NP_000457.1:p.Ala867Pro
NM_001282677.2:c.2428G>C	NP_001269606.1:p.Ala810Pro
NM_001282678.2:c.1975G>C	NP_001269607.1:p.Ala659Pro