Canonical Allele Identifier: CA456481430

Linked Data

MyVariant Identifiers: chr7:g.92123625G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494311G>A , CM000669.2:g.92494311G>A GRCh38
NC_000007.13:g.92123625G>A , CM000669.1:g.92123625G>A GRCh37
NC_000007.12:g.91961561G>A NCBI36
NG_008341.1:g.39221C>T
NG_008341.2:g.39221C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.3012C>T (PEX1) MANE Select ENSP00000248633.4:p.Tyr1004=
ENST00000248633.8:c.3012C>T (PEX1) ENSP00000248633.4:p.Tyr1004=
ENST00000428214.5:c.2841C>T (PEX1) ENSP00000394413.1:p.Tyr947=
ENST00000438045.5:c.2046C>T (PEX1) ENSP00000410438.1:p.Tyr682=
ENST00000484913.5:n.3051C>T (PEX1)
ENST00000496420.5:n.2904C>T (PEX1)
NM_000466.2:c.3012C>T (PEX1) NP_000457.1:p.Tyr1004=
NM_001282677.1:c.2841C>T (PEX1) NP_001269606.1:p.Tyr947=
NM_001282678.1:c.2388C>T (PEX1) NP_001269607.1:p.Tyr796=
XM_005250433.3:c.1263C>T (PEX1) XP_005250490.1:p.Tyr421=
XR_242246.3:n.3108C>T (PEX1)
XM_017012319.2:c.1263C>T (PEX1) XP_016867808.1:p.Tyr421=
XR_001744808.2:n.2039C>T (PEX1)
XR_001744843.2:n.5280G>A (GATAD1)
XR_242246.5:n.3059C>T (PEX1)
XR_927494.3:n.4131G>A (GATAD1)
XR_927503.3:n.4062G>A (GATAD1)
NM_000466.3:c.3012C>T (PEX1) MANE Select NP_000457.1:p.Tyr1004=
NM_001282677.2:c.2841C>T (PEX1) NP_001269606.1:p.Tyr947=
NM_001282678.2:c.2388C>T (PEX1) NP_001269607.1:p.Tyr796=