Canonical Allele Identifier: CA368183028

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92134078G>A (hg19) ; chr7:g.92504764G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92504764G>A , CM000669.2:g.92504764G>A	GRCh38
NC_000007.13:g.92134078G>A , CM000669.1:g.92134078G>A	GRCh37
NC_000007.12:g.91972014G>A	NCBI36
NG_008341.1:g.28768C>T
NG_008341.2:g.28768C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2039C>T MANE Select	ENSP00000248633.4:p.Pro680Leu
ENST00000248633.8:c.2039C>T	ENSP00000248633.4:p.Pro680Leu
ENST00000428214.5:c.1900+1484C>T	ENSP00000394413.1:n.1900+1484C>T
ENST00000438045.5:c.1073C>T	ENSP00000410438.1:p.Pro358Leu
ENST00000484913.5:n.2078C>T
ENST00000496420.5:n.1715C>T
NM_000466.2:c.2039C>T	NP_000457.1:p.Pro680Leu
NM_001282677.1:c.1900+1484C>T	NP_001269606.1:n.1900+1484C>T
NM_001282678.1:c.1415C>T	NP_001269607.1:p.Pro472Leu
XM_005250433.3:c.290C>T	XP_005250490.1:p.Pro97Leu
XR_242246.3:n.2135C>T
XM_017012319.2:c.290C>T	XP_016867808.1:p.Pro97Leu
XR_001744808.2:n.1066C>T
XR_242246.5:n.2086C>T
NM_000466.3:c.2039C>T MANE Select	NP_000457.1:p.Pro680Leu
NM_001282677.2:c.1900+1484C>T	NP_001269606.1:n.1900+1484C>T
NM_001282678.2:c.1415C>T	NP_001269607.1:p.Pro472Leu