Canonical Allele Identifier: CA2781901959
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117819959C>A , CM000670.2:g.117819959C>A GRCh38
NC_000008.10:g.118832198C>A , CM000670.1:g.118832198C>A GRCh37
NC_000008.9:g.118901379C>A NCBI36
NG_007455.2:g.296861G>T , LRG_493:g.296861G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684189.1:n.885-165G>T
ENST00000378204.7:c.1418-165G>T MANE Select ENSP00000367446.3:n.1418-165G>T
ENST00000378204.6:c.1418-165G>T ENSP00000367446.2:n.1418-165G>T
ENST00000437196.1:c.*309-165G>T ENSP00000407299.1:n.*309-165G>T
NM_000127.2:c.1418-165G>T , LRG_493t1:c.1418-165G>T NP_000118.2:n.1418-165G>T
NM_000127.3:c.1418-165G>T MANE Select NP_000118.2:n.1418-165G>T