Canonical Allele Identifier: CA368171125

Gene: PEX1

Linked Data

• MyVariant Identifiers: chr7:g.92126069T>G (hg19) ; chr7:g.92496755T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92496755T>G , CM000669.2:g.92496755T>G	GRCh38
NC_000007.13:g.92126069T>G , CM000669.1:g.92126069T>G	GRCh37
NC_000007.12:g.91964005T>G	NCBI36
NG_008341.1:g.36777A>C
NG_008341.2:g.36777A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2741A>C MANE Select	ENSP00000248633.4:p.Tyr914Ser
ENST00000248633.8:c.2741A>C	ENSP00000248633.4:p.Tyr914Ser
ENST00000428214.5:c.2570A>C	ENSP00000394413.1:p.Tyr857Ser
ENST00000438045.5:c.1775A>C	ENSP00000410438.1:p.Tyr592Ser
ENST00000484913.5:n.2780A>C
ENST00000496420.5:n.2633A>C
NM_000466.2:c.2741A>C	NP_000457.1:p.Tyr914Ser
NM_001282677.1:c.2570A>C	NP_001269606.1:p.Tyr857Ser
NM_001282678.1:c.2117A>C	NP_001269607.1:p.Tyr706Ser
XM_005250433.3:c.992A>C	XP_005250490.1:p.Tyr331Ser
XR_242246.3:n.2837A>C
XM_017012319.2:c.992A>C	XP_016867808.1:p.Tyr331Ser
XR_001744808.2:n.1768A>C
XR_242246.5:n.2788A>C
NM_000466.3:c.2741A>C MANE Select	NP_000457.1:p.Tyr914Ser
NM_001282677.2:c.2570A>C	NP_001269606.1:p.Tyr857Ser
NM_001282678.2:c.2117A>C	NP_001269607.1:p.Tyr706Ser