Canonical Allele Identifier: CA1813957397
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117837158C= , CM000670.2:g.117837158C= GRCh38
NC_000008.10:g.118849397C= , CM000670.1:g.118849397C= GRCh37
NC_000008.9:g.118918578C= NCBI36
NG_007455.2:g.279662G= , LRG_493:g.279662G=

Transcript Alleles

HGVS Amino-acid change
ENST00000684189.1:n.473G=
ENST00000378204.7:c.1006G= MANE Select ENSP00000367446.3:p.Val336=
ENST00000436216.2:c.374G=
ENST00000378204.6:c.1006G= ENSP00000367446.2:p.Val336=
ENST00000436216.1:c.374G=
ENST00000437196.1:c.74-1607G= ENSP00000407299.1:n.74-1607G=
NM_000127.2:c.1006G= , LRG_493t1:c.1006G= NP_000118.2:p.Val336=
NM_000127.3:c.1006G= MANE Select NP_000118.2:p.Val336=