Canonical Allele Identifier: CA2688347332
Gene: EXT1 HGNC NCBI

Linked Data

gnomAD v4: 8-118111434-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118111435del , CM000670.2:g.118111435del GRCh38
NC_000008.10:g.119123674del , CM000670.1:g.119123674del GRCh37
NC_000008.9:g.119192855del NCBI36
NG_007455.2:g.5385del , LRG_493:g.5385del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378204.7:c.-389del MANE Select ENSP00000367446.3:n.-389del
ENST00000378204.6:c.-389del ENSP00000367446.2:n.-389del
NM_000127.2:c.-389del , LRG_493t1:c.-389del NP_000118.2:n.-389del
NM_000127.3:c.-389del MANE Select NP_000118.2:n.-389del
Search 100 bp 5'
Search 100 bp 3'