Canonical Allele Identifier: CA456480986

Linked Data

MyVariant Identifiers: chr7:g.92120861T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491547T>A , CM000669.2:g.92491547T>A GRCh38
NC_000007.13:g.92120861T>A , CM000669.1:g.92120861T>A GRCh37
NC_000007.12:g.91958797T>A NCBI36
NG_008341.1:g.41985A>T
NG_008341.2:g.41985A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3208-45A>T (PEX1) MANE Select ENSP00000248633.4:n.3208-45A>T
ENST00000248633.8:c.3208-45A>T (PEX1) ENSP00000248633.4:n.3208-45A>T
ENST00000428214.5:c.3037-45A>T (PEX1) ENSP00000394413.1:n.3037-45A>T
ENST00000438045.5:c.2242-45A>T (PEX1) ENSP00000410438.1:n.2242-45A>T
ENST00000484913.5:n.3247-45A>T (PEX1)
ENST00000496420.5:n.4263-45A>T (PEX1)
NM_000466.2:c.3208-45A>T (PEX1) NP_000457.1:n.3208-45A>T
NM_001282677.1:c.3037-45A>T (PEX1) NP_001269606.1:n.3037-45A>T
NM_001282678.1:c.2584-45A>T (PEX1) NP_001269607.1:n.2584-45A>T
XM_005250433.3:c.1459-45A>T (PEX1) XP_005250490.1:n.1459-45A>T
XR_242246.3:n.3304-45A>T (PEX1)
XM_017012319.2:c.1459-45A>T (PEX1) XP_016867808.1:n.1459-45A>T
XR_001744808.2:n.2235-45A>T (PEX1)
XR_001744842.2:n.2585T>A (GATAD1)
XR_001744843.2:n.2516T>A (GATAD1)
XR_002956472.1:n.2642T>A (GATAD1)
XR_002956473.1:n.2673T>A (GATAD1)
XR_002956474.1:n.2590T>A (GATAD1)
XR_242246.5:n.3255-45A>T (PEX1)
XR_927494.3:n.1367T>A (GATAD1)
XR_927500.3:n.1364T>A (GATAD1)
XR_927503.3:n.1298T>A (GATAD1)
NM_000466.3:c.3208-45A>T (PEX1) MANE Select NP_000457.1:n.3208-45A>T
NM_001282677.2:c.3037-45A>T (PEX1) NP_001269606.1:n.3037-45A>T
NM_001282678.2:c.2584-45A>T (PEX1) NP_001269607.1:n.2584-45A>T