Canonical Allele Identifier: CA371893389

Gene: EXT1

Linked Data

• MyVariant Identifiers: chr8:g.118849433A>T (hg19) ; chr8:g.117837194A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117837194A>T , CM000670.2:g.117837194A>T	GRCh38
NC_000008.10:g.118849433A>T , CM000670.1:g.118849433A>T	GRCh37
NC_000008.9:g.118918614A>T	NCBI36
NG_007455.2:g.279626T>A , LRG_493:g.279626T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684189.1:n.437T>A
ENST00000378204.7:c.970T>A MANE Select	ENSP00000367446.3:p.Tyr324Asn
ENST00000436216.2:c.338T>A
ENST00000378204.6:c.970T>A	ENSP00000367446.2:p.Tyr324Asn
ENST00000436216.1:c.338T>A
ENST00000437196.1:c.74-1643T>A	ENSP00000407299.1:n.74-1643T>A
NM_000127.2:c.970T>A , LRG_493t1:c.970T>A	NP_000118.2:p.Tyr324Asn
NM_000127.3:c.970T>A MANE Select	NP_000118.2:p.Tyr324Asn