Canonical Allele Identifier: CA1814090465
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118111462G= , CM000670.2:g.118111462G= GRCh38
NC_000008.10:g.119123701G= , CM000670.1:g.119123701G= GRCh37
NC_000008.9:g.119192882G= NCBI36
NG_007455.2:g.5358C= , LRG_493:g.5358C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378204.7:c.-416C= MANE Select ENSP00000367446.3:n.-416C=
ENST00000378204.6:c.-416C= ENSP00000367446.2:n.-416C=
NM_000127.2:c.-416C= , LRG_493t1:c.-416C= NP_000118.2:n.-416C=
NM_000127.3:c.-416C= MANE Select NP_000118.2:n.-416C=