Canonical Allele Identifier: CA1813915722
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117807285C= , CM000670.2:g.117807285C= GRCh38
NC_000008.10:g.118819524C= , CM000670.1:g.118819524C= GRCh37
NC_000008.9:g.118888705C= NCBI36
NG_007455.2:g.309535G= , LRG_493:g.309535G=

Transcript Alleles

HGVS Amino-acid change
ENST00000684189.1:n.1282G=
ENST00000378204.7:c.1815G= MANE Select ENSP00000367446.3:p.Arg605=
ENST00000378204.6:c.1815G= ENSP00000367446.2:p.Arg605=
ENST00000437196.1:c.*706G= ENSP00000407299.1:n.*706G=
NM_000127.2:c.1815G= , LRG_493t1:c.1815G= NP_000118.2:p.Arg605=
NM_000127.3:c.1815G= MANE Select NP_000118.2:p.Arg605=