Canonical Allele Identifier: CA371892122

Gene: EXT1

Linked Data

• MyVariant Identifiers: chr8:g.118847721G>C (hg19) ; chr8:g.117835482G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117835482G>C , CM000670.2:g.117835482G>C	GRCh38
NC_000008.10:g.118847721G>C , CM000670.1:g.118847721G>C	GRCh37
NC_000008.9:g.118916902G>C	NCBI36
NG_007455.2:g.281338C>G , LRG_493:g.281338C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684189.1:n.593C>G
ENST00000378204.7:c.1126C>G MANE Select	ENSP00000367446.3:p.Gln376Glu
ENST00000436216.2:c.494C>G
ENST00000378204.6:c.1126C>G	ENSP00000367446.2:p.Gln376Glu
ENST00000436216.1:c.494C>G
ENST00000437196.1:c.*17C>G	ENSP00000407299.1:n.*17C>G
NM_000127.2:c.1126C>G , LRG_493t1:c.1126C>G	NP_000118.2:p.Gln376Glu
NM_000127.3:c.1126C>G MANE Select	NP_000118.2:p.Gln376Glu