Canonical Allele Identifier: CA371878152
Gene: EXT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.118819516T>G (hg19) chr8:g.117807277T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117807277T>G , CM000670.2:g.117807277T>G GRCh38
NC_000008.10:g.118819516T>G , CM000670.1:g.118819516T>G GRCh37
NC_000008.9:g.118888697T>G NCBI36
NG_007455.2:g.309543A>C , LRG_493:g.309543A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000684189.1:n.1290A>C
ENST00000378204.7:c.1823A>C MANE Select ENSP00000367446.3:p.Tyr608Ser
ENST00000378204.6:c.1823A>C ENSP00000367446.2:p.Tyr608Ser
ENST00000437196.1:c.*714A>C ENSP00000407299.1:n.*714A>C
NM_000127.2:c.1823A>C , LRG_493t1:c.1823A>C NP_000118.2:p.Tyr608Ser
NM_000127.3:c.1823A>C MANE Select NP_000118.2:p.Tyr608Ser
Search 100 bp 5'
Search 100 bp 3'