Canonical Allele Identifier: CA371892632

Gene: EXT1

Linked Data

• MyVariant Identifiers: chr8:g.118847765C>G (hg19) ; chr8:g.117835526C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117835526C>G , CM000670.2:g.117835526C>G	GRCh38
NC_000008.10:g.118847765C>G , CM000670.1:g.118847765C>G	GRCh37
NC_000008.9:g.118916946C>G	NCBI36
NG_007455.2:g.281294G>C , LRG_493:g.281294G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684189.1:n.549G>C
ENST00000378204.7:c.1082G>C MANE Select	ENSP00000367446.3:p.Ser361Thr
ENST00000436216.2:c.450G>C
ENST00000378204.6:c.1082G>C	ENSP00000367446.2:p.Ser361Thr
ENST00000436216.1:c.450G>C
ENST00000437196.1:c.99G>C	ENSP00000407299.1:p.Gln33His
NM_000127.2:c.1082G>C , LRG_493t1:c.1082G>C	NP_000118.2:p.Ser361Thr
NM_000127.3:c.1082G>C MANE Select	NP_000118.2:p.Ser361Thr