Canonical Allele Identifier: CA462468837

Gene: EXT1

Linked Data

• dbSNP Id: rs146407591
• MyVariant Identifiers: chr8:g.118847746T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117835507T>G , CM000670.2:g.117835507T>G	GRCh38
NC_000008.10:g.118847746T>G , CM000670.1:g.118847746T>G	GRCh37
NC_000008.9:g.118916927T>G	NCBI36
NG_007455.2:g.281313A>C , LRG_493:g.281313A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684189.1:n.568A>C
ENST00000378204.7:c.1101A>C MANE Select	ENSP00000367446.3:p.Pro367=
ENST00000436216.2:c.469A>C
ENST00000378204.6:c.1101A>C	ENSP00000367446.2:p.Pro367=
ENST00000436216.1:c.469A>C
ENST00000437196.1:c.118A>C	ENSP00000407299.1:p.Ile40Leu
NM_000127.2:c.1101A>C , LRG_493t1:c.1101A>C	NP_000118.2:p.Pro367=
NM_000127.3:c.1101A>C MANE Select	NP_000118.2:p.Pro367=