Canonical Allele Identifier: CA1814090590
Gene: EXT1 HGNC NCBI

Linked Data

dbSNP Id: rs1817905070

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118111607dup , CM000670.2:g.118111607dup GRCh38
NC_000008.10:g.119123846dup , CM000670.1:g.119123846dup GRCh37
NC_000008.9:g.119193027dup NCBI36
NG_007455.2:g.5215dup , LRG_493:g.5215dup

Transcript Alleles

HGVS Amino-acid change
ENST00000378204.7:c.-559dup MANE Select ENSP00000367446.3:n.-559dup
ENST00000378204.6:c.-559dup ENSP00000367446.2:n.-559dup
NM_000127.2:c.-559dup , LRG_493t1:c.-559dup NP_000118.2:n.-559dup
NM_000127.3:c.-559dup MANE Select NP_000118.2:n.-559dup