Canonical Allele Identifier: CA371892004

Gene: EXT1

Linked Data

• MyVariant Identifiers: chr8:g.118847708A>G (hg19) ; chr8:g.117835469A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117835469A>G , CM000670.2:g.117835469A>G	GRCh38
NC_000008.10:g.118847708A>G , CM000670.1:g.118847708A>G	GRCh37
NC_000008.9:g.118916889A>G	NCBI36
NG_007455.2:g.281351T>C , LRG_493:g.281351T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684189.1:n.606T>C
ENST00000378204.7:c.1139T>C MANE Select	ENSP00000367446.3:p.Ile380Thr
ENST00000436216.2:c.507T>C
ENST00000378204.6:c.1139T>C	ENSP00000367446.2:p.Ile380Thr
ENST00000436216.1:c.507T>C
ENST00000437196.1:c.*30T>C	ENSP00000407299.1:n.*30T>C
NM_000127.2:c.1139T>C , LRG_493t1:c.1139T>C	NP_000118.2:p.Ile380Thr
NM_000127.3:c.1139T>C MANE Select	NP_000118.2:p.Ile380Thr