Canonical Allele Identifier: CA2695207084
Gene: PEX7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.136898142_136898241del , CM000668.2:g.136898142_136898241del GRCh38
NC_000006.11:g.137219280_137219379del , CM000668.1:g.137219280_137219379del GRCh37
NC_000006.10:g.137260973_137261072del NCBI36
NG_008462.1:g.80563_80662del

Transcript Alleles

HGVS Amino-acid Change
ENST00000318471.5:c.804_903del
ENST00000541292.6:c.*69_*168del
ENST00000678002.1:c.492_591del
ENST00000678557.1:c.690_789del
ENST00000679286.1:c.684_783del
ENST00000318471.4:c.804_903del
NM_000288.3:c.804_903del
XM_005267019.3:c.690_789del
XM_006715502.1:c.510_609del
XM_005267019.4:c.690_789del
XM_006715502.2:c.510_609del
XM_017010934.2:c.527_*26del
NM_000288.4:c.804_903del