Canonical Allele Identifier: CA1813957367
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117837106A= , CM000670.2:g.117837106A= GRCh38
NC_000008.10:g.118849345A= , CM000670.1:g.118849345A= GRCh37
NC_000008.9:g.118918526A= NCBI36
NG_007455.2:g.279714T= , LRG_493:g.279714T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684189.1:n.523+2T=
ENST00000378204.7:c.1056+2T= MANE Select ENSP00000367446.3:n.1056+2T=
ENST00000436216.2:c.424+2T=
ENST00000378204.6:c.1056+2T= ENSP00000367446.2:n.1056+2T=
ENST00000436216.1:c.424+2T=
ENST00000437196.1:c.74-1555T= ENSP00000407299.1:n.74-1555T=
NM_000127.2:c.1056+2T= , LRG_493t1:c.1056+2T= NP_000118.2:n.1056+2T=
NM_000127.3:c.1056+2T= MANE Select NP_000118.2:n.1056+2T=