Canonical Allele Identifier: CA462468880

Gene: EXT1

Linked Data

• MyVariant Identifiers: chr8:g.118847788A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117835549A>T , CM000670.2:g.117835549A>T	GRCh38
NC_000008.10:g.118847788A>T , CM000670.1:g.118847788A>T	GRCh37
NC_000008.9:g.118916969A>T	NCBI36
NG_007455.2:g.281271T>A , LRG_493:g.281271T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684189.1:n.526T>A
ENST00000378204.7:c.1059T>A MANE Select	ENSP00000367446.3:p.Ala353=
ENST00000436216.2:c.427T>A
ENST00000378204.6:c.1059T>A	ENSP00000367446.2:p.Ala353=
ENST00000436216.1:c.427T>A
ENST00000437196.1:c.76T>A	ENSP00000407299.1:p.Cys26Ser
NM_000127.2:c.1059T>A , LRG_493t1:c.1059T>A	NP_000118.2:p.Ala353=
NM_000127.3:c.1059T>A MANE Select	NP_000118.2:p.Ala353=