Canonical Allele Identifier: CA368168479

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494531A>C , CM000669.2:g.92494531A>C GRCh38
NC_000007.13:g.92123845A>C , CM000669.1:g.92123845A>C GRCh37
NC_000007.12:g.91961781A>C NCBI36
NG_008341.1:g.39001T>G
NG_008341.2:g.39001T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2882T>G (PEX1) MANE Select ENSP00000248633.4:p.Val961Gly
ENST00000248633.8:c.2882T>G (PEX1) ENSP00000248633.4:p.Val961Gly
ENST00000428214.5:c.2711T>G (PEX1) ENSP00000394413.1:p.Val904Gly
ENST00000438045.5:c.1916T>G (PEX1) ENSP00000410438.1:p.Val639Gly
ENST00000484913.5:n.2921T>G (PEX1)
ENST00000496420.5:n.2774T>G (PEX1)
NM_000466.2:c.2882T>G (PEX1) NP_000457.1:p.Val961Gly
NM_001282677.1:c.2711T>G (PEX1) NP_001269606.1:p.Val904Gly
NM_001282678.1:c.2258T>G (PEX1) NP_001269607.1:p.Val753Gly
XM_005250433.3:c.1133T>G (PEX1) XP_005250490.1:p.Val378Gly
XR_242246.3:n.2978T>G (PEX1)
XM_017012319.2:c.1133T>G (PEX1) XP_016867808.1:p.Val378Gly
XR_001744808.2:n.1909T>G (PEX1)
XR_001744843.2:n.5500A>C (GATAD1)
XR_242246.5:n.2929T>G (PEX1)
XR_927494.3:n.4351A>C (GATAD1)
XR_927503.3:n.4282A>C (GATAD1)
NM_000466.3:c.2882T>G (PEX1) MANE Select NP_000457.1:p.Val961Gly
NM_001282677.2:c.2711T>G (PEX1) NP_001269606.1:p.Val904Gly
NM_001282678.2:c.2258T>G (PEX1) NP_001269607.1:p.Val753Gly