Canonical Allele Identifier: CA2680490686
Gene: PEX7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.136872181_136872182insTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000668.2:g.136872181_136872182insTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000006.11:g.137193319_137193320insTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000668.1:g.137193319_137193320insTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000006.10:g.137235012_137235013insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NCBI36
NG_008462.1:g.54602_54603insTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000318471.5:c.748-17_748-16insTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000315680.3:n.748-17_748-16insTTTTT...
ENST00000541292.6:c.*13-17_*13-16insTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000441004.1:n.*13-17_*13-16insTTTTT...
ENST00000678002.1:c.436-17_436-16insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000678557.1:c.634-17_634-16insTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000502962.1:n.634-17_634-16insTTTTT...
ENST00000678593.1:c.753-17_753-16insTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000503841.1:n.753-17_753-16insTTTTT...
ENST00000679286.1:c.628-17_628-16insTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000503168.1:n.628-17_628-16insTTTTT...
ENST00000318471.4:c.748-17_748-16insTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000315680.3:n.748-17_748-16insTTTTT...
NM_000288.3:c.748-17_748-16insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_000279.1:n.748-17_748-16insTTTTTTTTTTT...
XM_005267019.3:c.634-17_634-16insTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_005267076.1:n.634-17_634-16insTTTTTTTT...
XM_006715502.1:c.454-17_454-16insTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_006715565.1:n.454-17_454-16insTTTTTTTT...
XM_011535900.1:c.527-25961_527-25960insTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011534202.1:n.527-25961_527-25960insTT...
XM_005267019.4:c.634-17_634-16insTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_005267076.1:n.634-17_634-16insTTTTTTTT...
XM_006715502.2:c.454-17_454-16insTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_006715565.1:n.454-17_454-16insTTTTTTTT...
XM_017010934.2:c.527-25961_527-25960insTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_016866423.1:n.527-25961_527-25960insTT...
NM_000288.4:c.748-17_748-16insTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_000279.1:n.748-17_748-16insTTTTTTTTTTT...