Canonical Allele Identifier: CA4017748
Gene: PEX7 HGNC NCBI

Linked Data

dbSNP Id: rs746730895

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.136872194_136872197del , CM000668.2:g.136872194_136872197del GRCh38
NC_000006.11:g.137193332_137193335del , CM000668.1:g.137193332_137193335del GRCh37
NC_000006.10:g.137235025_137235028del NCBI36
NG_008462.1:g.54615_54618del

Transcript Alleles

HGVS Amino-acid change
ENST00000318471.5:c.748-4_748-1del MANE Select ENSP00000315680.3:n.748-4_748-1del
ENST00000541292.6:c.*13-4_*13-1del ENSP00000441004.1:n.*13-4_*13-1del
ENST00000678002.1:c.436-4_436-1del
ENST00000678557.1:c.634-4_634-1del ENSP00000502962.1:n.634-4_634-1del
ENST00000678593.1:c.753-4_753-1del ENSP00000503841.1:n.753-4_753-1del
ENST00000679286.1:c.628-4_628-1del ENSP00000503168.1:n.628-4_628-1del
ENST00000318471.4:c.748-4_748-1del ENSP00000315680.3:n.748-4_748-1del
NM_000288.3:c.748-4_748-1del NP_000279.1:n.748-4_748-1del
XM_005267019.3:c.634-4_634-1del XP_005267076.1:n.634-4_634-1del
XM_006715502.1:c.454-4_454-1del XP_006715565.1:n.454-4_454-1del
XM_011535900.1:c.527-25948_527-25945del XP_011534202.1:n.527-25948_527-25945del
XM_005267019.4:c.634-4_634-1del XP_005267076.1:n.634-4_634-1del
XM_006715502.2:c.454-4_454-1del XP_006715565.1:n.454-4_454-1del
XM_017010934.2:c.527-25948_527-25945del XP_016866423.1:n.527-25948_527-25945del
NM_000288.4:c.748-4_748-1del MANE Select NP_000279.1:n.748-4_748-1del