Canonical Allele Identifier: CA1814090589
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118111605T= , CM000670.2:g.118111605T= GRCh38
NC_000008.10:g.119123844T= , CM000670.1:g.119123844T= GRCh37
NC_000008.9:g.119193025T= NCBI36
NG_007455.2:g.5215A= , LRG_493:g.5215A=

Transcript Alleles

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