Canonical Allele Identifier: CA385987639
Gene: DUSP6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.89744560A>C (hg19) chr12:g.89350783A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.89350783A>C , CM000674.2:g.89350783A>C GRCh38
NC_000012.11:g.89744560A>C , CM000674.1:g.89744560A>C GRCh37
NC_000012.10:g.88268691A>C NCBI36
NG_033915.1:g.7077T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000279488.8:c.643T>G MANE Select ENSP00000279488.6:p.Tyr215Asp
ENST00000279488.7:c.643T>G ENSP00000279488.6:p.Tyr215Asp
ENST00000308385.6:c.400+857T>G ENSP00000307835.6:n.400+857T>G
ENST00000547140.1:n.329T>G
ENST00000547291.1:c.268T>G ENSP00000449838.1:p.Tyr90Asp
NM_001946.3:c.643T>G NP_001937.2:p.Tyr215Asp
NM_022652.3:c.400+857T>G NP_073143.2:n.400+857T>G
NM_001946.4:c.643T>G MANE Select NP_001937.2:p.Tyr215Asp
NM_022652.4:c.400+857T>G NP_073143.2:n.400+857T>G
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