Canonical Allele Identifier: CA385988029
Gene: DUSP6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.89744625T>G (hg19) chr12:g.89350848T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.89350848T>G , CM000674.2:g.89350848T>G GRCh38
NC_000012.11:g.89744625T>G , CM000674.1:g.89744625T>G GRCh37
NC_000012.10:g.88268756T>G NCBI36
NG_033915.1:g.7012A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000279488.8:c.578A>C MANE Select ENSP00000279488.6:p.Asp193Ala
ENST00000279488.7:c.578A>C ENSP00000279488.6:p.Asp193Ala
ENST00000308385.6:c.400+792A>C ENSP00000307835.6:n.400+792A>C
ENST00000547140.1:n.264A>C
ENST00000547291.1:c.203A>C ENSP00000449838.1:p.Asp68Ala
NM_001946.3:c.578A>C NP_001937.2:p.Asp193Ala
NM_022652.3:c.400+792A>C NP_073143.2:n.400+792A>C
NM_001946.4:c.578A>C MANE Select NP_001937.2:p.Asp193Ala
NM_022652.4:c.400+792A>C NP_073143.2:n.400+792A>C
Search 100 bp 5'
Search 100 bp 3'