Canonical Allele Identifier: CA368170862

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92126034A>C (hg19) ; chr7:g.92496720A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92496720A>C , CM000669.2:g.92496720A>C	GRCh38
NC_000007.13:g.92126034A>C , CM000669.1:g.92126034A>C	GRCh37
NC_000007.12:g.91963970A>C	NCBI36
NG_008341.1:g.36812T>G
NG_008341.2:g.36812T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2776T>G MANE Select	ENSP00000248633.4:p.Phe926Val
ENST00000248633.8:c.2776T>G	ENSP00000248633.4:p.Phe926Val
ENST00000428214.5:c.2605T>G	ENSP00000394413.1:p.Phe869Val
ENST00000438045.5:c.1810T>G	ENSP00000410438.1:p.Phe604Val
ENST00000484913.5:n.2815T>G
ENST00000496420.5:n.2668T>G
NM_000466.2:c.2776T>G	NP_000457.1:p.Phe926Val
NM_001282677.1:c.2605T>G	NP_001269606.1:p.Phe869Val
NM_001282678.1:c.2152T>G	NP_001269607.1:p.Phe718Val
XM_005250433.3:c.1027T>G	XP_005250490.1:p.Phe343Val
XR_242246.3:n.2872T>G
XM_017012319.2:c.1027T>G	XP_016867808.1:p.Phe343Val
XR_001744808.2:n.1803T>G
XR_242246.5:n.2823T>G
NM_000466.3:c.2776T>G MANE Select	NP_000457.1:p.Phe926Val
NM_001282677.2:c.2605T>G	NP_001269606.1:p.Phe869Val
NM_001282678.2:c.2152T>G	NP_001269607.1:p.Phe718Val