Canonical Allele Identifier: CA1814090587
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118111604C= , CM000670.2:g.118111604C= GRCh38
NC_000008.10:g.119123843C= , CM000670.1:g.119123843C= GRCh37
NC_000008.9:g.119193024C= NCBI36
NG_007455.2:g.5216G= , LRG_493:g.5216G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378204.7:c.-558G= MANE Select ENSP00000367446.3:n.-558G=
ENST00000378204.6:c.-558G= ENSP00000367446.2:n.-558G=
NM_000127.2:c.-558G= , LRG_493t1:c.-558G= NP_000118.2:n.-558G=
NM_000127.3:c.-558G= MANE Select NP_000118.2:n.-558G=