Canonical Allele Identifier: CA1814090467
Gene: EXT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118111463A= , CM000670.2:g.118111463A= GRCh38
NC_000008.10:g.119123702A= , CM000670.1:g.119123702A= GRCh37
NC_000008.9:g.119192883A= NCBI36
NG_007455.2:g.5357T= , LRG_493:g.5357T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378204.7:c.-417T= MANE Select ENSP00000367446.3:n.-417T=
ENST00000378204.6:c.-417T= ENSP00000367446.2:n.-417T=
NM_000127.2:c.-417T= , LRG_493t1:c.-417T= NP_000118.2:n.-417T=
NM_000127.3:c.-417T= MANE Select NP_000118.2:n.-417T=
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