Canonical Allele Identifier: CA1813949891
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117819787C= , CM000670.2:g.117819787C= GRCh38
NC_000008.10:g.118832026C= , CM000670.1:g.118832026C= GRCh37
NC_000008.9:g.118901207C= NCBI36
NG_007455.2:g.297033G= , LRG_493:g.297033G=

Transcript Alleles

HGVS Amino-acid change
ENST00000684189.1:n.892G=
ENST00000378204.7:c.1425G= MANE Select ENSP00000367446.3:p.Lys475=
ENST00000378204.6:c.1425G= ENSP00000367446.2:p.Lys475=
ENST00000437196.1:c.*316G= ENSP00000407299.1:n.*316G=
NM_000127.2:c.1425G= , LRG_493t1:c.1425G= NP_000118.2:p.Lys475=
NM_000127.3:c.1425G= MANE Select NP_000118.2:p.Lys475=