Canonical Allele Identifier: CA1814088361
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118110105T= , CM000670.2:g.118110105T= GRCh38
NC_000008.10:g.119122344T= , CM000670.1:g.119122344T= GRCh37
NC_000008.9:g.119191525T= NCBI36
NG_007455.2:g.6715A= , LRG_493:g.6715A=

Transcript Alleles

HGVS Amino-acid change
ENST00000378204.7:c.942A= MANE Select ENSP00000367446.3:p.Arg314=
ENST00000436216.2:c.310A=
ENST00000378204.6:c.942A= ENSP00000367446.2:p.Arg314=
ENST00000436216.1:c.310A=
ENST00000437196.1:c.73+869A= ENSP00000407299.1:n.73+869A=
NM_000127.2:c.942A= , LRG_493t1:c.942A= NP_000118.2:p.Arg314=
NM_000127.3:c.942A= MANE Select NP_000118.2:p.Arg314=