Canonical Allele Identifier: CA1814090477
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118111476C= , CM000670.2:g.118111476C= GRCh38
NC_000008.10:g.119123715C= , CM000670.1:g.119123715C= GRCh37
NC_000008.9:g.119192896C= NCBI36
NG_007455.2:g.5344G= , LRG_493:g.5344G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378204.7:c.-430G= MANE Select ENSP00000367446.3:n.-430G=
ENST00000378204.6:c.-430G= ENSP00000367446.2:n.-430G=
NM_000127.2:c.-430G= , LRG_493t1:c.-430G= NP_000118.2:n.-430G=
NM_000127.3:c.-430G= MANE Select NP_000118.2:n.-430G=