Canonical Allele Identifier: CA1814090469
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118111466C= , CM000670.2:g.118111466C= GRCh38
NC_000008.10:g.119123705C= , CM000670.1:g.119123705C= GRCh37
NC_000008.9:g.119192886C= NCBI36
NG_007455.2:g.5354G= , LRG_493:g.5354G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378204.7:c.-420G= MANE Select ENSP00000367446.3:n.-420G=
ENST00000378204.6:c.-420G= ENSP00000367446.2:n.-420G=
NM_000127.2:c.-420G= , LRG_493t1:c.-420G= NP_000118.2:n.-420G=
NM_000127.3:c.-420G= MANE Select NP_000118.2:n.-420G=