Canonical Allele Identifier: CA371877884

Gene: EXT1

Linked Data

• MyVariant Identifiers: chr8:g.118819462T>G (hg19) ; chr8:g.117807223T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117807223T>G , CM000670.2:g.117807223T>G	GRCh38
NC_000008.10:g.118819462T>G , CM000670.1:g.118819462T>G	GRCh37
NC_000008.9:g.118888643T>G	NCBI36
NG_007455.2:g.309597A>C , LRG_493:g.309597A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684189.1:n.1344A>C
ENST00000378204.7:c.1877A>C MANE Select	ENSP00000367446.3:p.Tyr626Ser
ENST00000378204.6:c.1877A>C	ENSP00000367446.2:p.Tyr626Ser
ENST00000437196.1:c.*768A>C	ENSP00000407299.1:n.*768A>C
NM_000127.2:c.1877A>C , LRG_493t1:c.1877A>C	NP_000118.2:p.Tyr626Ser
NM_000127.3:c.1877A>C MANE Select	NP_000118.2:p.Tyr626Ser