Canonical Allele Identifier: CA1814090878
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118111790G= , CM000670.2:g.118111790G= GRCh38
NC_000008.10:g.119124029G= , CM000670.1:g.119124029G= GRCh37
NC_000008.9:g.119193210G= NCBI36
NG_007455.2:g.5030C= , LRG_493:g.5030C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378204.7:c.-744C= MANE Select ENSP00000367446.3:n.-744C=
ENST00000378204.6:c.-744C= ENSP00000367446.2:n.-744C=
NM_000127.2:c.-744C= , LRG_493t1:c.-744C= NP_000118.2:n.-744C=
NM_000127.3:c.-744C= MANE Select NP_000118.2:n.-744C=