Canonical Allele Identifier: CA4017740
Gene: PEX7 HGNC NCBI

Linked Data

dbSNP Id: rs1554334018

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.136872171_136872172insGT , CM000668.2:g.136872171_136872172insGT GRCh38
NC_000006.11:g.137193309_137193310insGT , CM000668.1:g.137193309_137193310insGT GRCh37
NC_000006.10:g.137235002_137235003insGT NCBI36
NG_008462.1:g.54592_54593insGT

Transcript Alleles

HGVS Amino-acid change
ENST00000318471.5:c.748-27_748-26insGT MANE Select ENSP00000315680.3:n.748-27_748-26insGT
ENST00000541292.6:c.*13-27_*13-26insGT ENSP00000441004.1:n.*13-27_*13-26insGT
ENST00000678002.1:c.436-27_436-26insGT
ENST00000678557.1:c.634-27_634-26insGT ENSP00000502962.1:n.634-27_634-26insGT
ENST00000678593.1:c.753-27_753-26insGT ENSP00000503841.1:n.753-27_753-26insGT
ENST00000679286.1:c.628-27_628-26insGT ENSP00000503168.1:n.628-27_628-26insGT
ENST00000318471.4:c.748-27_748-26insGT ENSP00000315680.3:n.748-27_748-26insGT
NM_000288.3:c.748-27_748-26insGT NP_000279.1:n.748-27_748-26insGT
XM_005267019.3:c.634-27_634-26insGT XP_005267076.1:n.634-27_634-26insGT
XM_006715502.1:c.454-27_454-26insGT XP_006715565.1:n.454-27_454-26insGT
XM_011535900.1:c.527-25971_527-25970insGT XP_011534202.1:n.527-25971_527-25970insGT...
XM_005267019.4:c.634-27_634-26insGT XP_005267076.1:n.634-27_634-26insGT
XM_006715502.2:c.454-27_454-26insGT XP_006715565.1:n.454-27_454-26insGT
XM_017010934.2:c.527-25971_527-25970insGT XP_016866423.1:n.527-25971_527-25970insGT...
NM_000288.4:c.748-27_748-26insGT MANE Select NP_000279.1:n.748-27_748-26insGT