Canonical Allele Identifier: CA2776945588

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491583_92491584insAGA , CM000669.2:g.92491583_92491584insAGA GRCh38
NC_000007.13:g.92120897_92120898insAGA , CM000669.1:g.92120897_92120898insAGA GRCh37
NC_000007.12:g.91958833_91958834insAGA NCBI36
NG_008341.1:g.41948_41949insTCT
NG_008341.2:g.41948_41949insTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3208-82_3208-81insTCT (PEX1) MANE Select ENSP00000248633.4:n.3208-82_3208-81insTCT
ENST00000248633.8:c.3208-82_3208-81insTCT (PEX1) ENSP00000248633.4:n.3208-82_3208-81insTCT
ENST00000428214.5:c.3037-82_3037-81insTCT (PEX1) ENSP00000394413.1:n.3037-82_3037-81insTCT
ENST00000438045.5:c.2242-82_2242-81insTCT (PEX1) ENSP00000410438.1:n.2242-82_2242-81insTCT
ENST00000484913.5:n.3247-82_3247-81insTCT (PEX1)
ENST00000496420.5:n.4263-82_4263-81insTCT (PEX1)
NM_000466.2:c.3208-82_3208-81insTCT (PEX1) NP_000457.1:n.3208-82_3208-81insTCT
NM_001282677.1:c.3037-82_3037-81insTCT (PEX1) NP_001269606.1:n.3037-82_3037-81insTCT
NM_001282678.1:c.2584-82_2584-81insTCT (PEX1) NP_001269607.1:n.2584-82_2584-81insTCT
XM_005250433.3:c.1459-82_1459-81insTCT (PEX1) XP_005250490.1:n.1459-82_1459-81insTCT
XR_242246.3:n.3304-82_3304-81insTCT (PEX1)
XM_017012319.2:c.1459-82_1459-81insTCT (PEX1) XP_016867808.1:n.1459-82_1459-81insTCT
XR_001744808.2:n.2235-82_2235-81insTCT (PEX1)
XR_001744842.2:n.2621_2622insAGA (GATAD1)
XR_001744843.2:n.2552_2553insAGA (GATAD1)
XR_002956472.1:n.2678_2679insAGA (GATAD1)
XR_002956473.1:n.2709_2710insAGA (GATAD1)
XR_002956474.1:n.2626_2627insAGA (GATAD1)
XR_242246.5:n.3255-82_3255-81insTCT (PEX1)
XR_927494.3:n.1403_1404insAGA (GATAD1)
XR_927500.3:n.1400_1401insAGA (GATAD1)
XR_927503.3:n.1334_1335insAGA (GATAD1)
NM_000466.3:c.3208-82_3208-81insTCT (PEX1) MANE Select NP_000457.1:n.3208-82_3208-81insTCT
NM_001282677.2:c.3037-82_3037-81insTCT (PEX1) NP_001269606.1:n.3037-82_3037-81insTCT
NM_001282678.2:c.2584-82_2584-81insTCT (PEX1) NP_001269607.1:n.2584-82_2584-81insTCT