Canonical Allele Identifier: CA481304528
Gene: DUSP6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.89744657A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.89350880A>C , CM000674.2:g.89350880A>C GRCh38
NC_000012.11:g.89744657A>C , CM000674.1:g.89744657A>C GRCh37
NC_000012.10:g.88268788A>C NCBI36
NG_033915.1:g.6980T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000279488.8:c.546T>G MANE Select ENSP00000279488.6:p.Ser182=
ENST00000279488.7:c.546T>G ENSP00000279488.6:p.Ser182=
ENST00000308385.6:c.400+760T>G ENSP00000307835.6:n.400+760T>G
ENST00000547140.1:n.232T>G
ENST00000547291.1:c.171T>G ENSP00000449838.1:p.Ser57=
NM_001946.3:c.546T>G NP_001937.2:p.Ser182=
NM_022652.3:c.400+760T>G NP_073143.2:n.400+760T>G
NM_001946.4:c.546T>G MANE Select NP_001937.2:p.Ser182=
NM_022652.4:c.400+760T>G NP_073143.2:n.400+760T>G
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