Canonical Allele Identifier: CA371891888

Gene: EXT1

Linked Data

• MyVariant Identifiers: chr8:g.118847695T>A (hg19) ; chr8:g.117835456T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117835456T>A , CM000670.2:g.117835456T>A	GRCh38
NC_000008.10:g.118847695T>A , CM000670.1:g.118847695T>A	GRCh37
NC_000008.9:g.118916876T>A	NCBI36
NG_007455.2:g.281364A>T , LRG_493:g.281364A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684189.1:n.619A>T
ENST00000378204.7:c.1152A>T MANE Select	ENSP00000367446.3:p.Arg384Ser
ENST00000436216.2:c.520A>T
ENST00000378204.6:c.1152A>T	ENSP00000367446.2:p.Arg384Ser
ENST00000436216.1:c.520A>T
ENST00000437196.1:c.*43A>T	ENSP00000407299.1:n.*43A>T
NM_000127.2:c.1152A>T , LRG_493t1:c.1152A>T	NP_000118.2:p.Arg384Ser
NM_000127.3:c.1152A>T MANE Select	NP_000118.2:p.Arg384Ser