Canonical Allele Identifier: CA385987502
Gene: DUSP6 HGNC NCBI

Linked Data

gnomAD v4: 12-89350768-T-C
MyVariant Identifiers: chr12:g.89744545T>C (hg19) chr12:g.89350768T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.89350768T>C , CM000674.2:g.89350768T>C GRCh38
NC_000012.11:g.89744545T>C , CM000674.1:g.89744545T>C GRCh37
NC_000012.10:g.88268676T>C NCBI36
NG_033915.1:g.7092A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000279488.8:c.658A>G MANE Select ENSP00000279488.6:p.Lys220Glu
ENST00000279488.7:c.658A>G ENSP00000279488.6:p.Lys220Glu
ENST00000308385.6:c.400+872A>G ENSP00000307835.6:n.400+872A>G
ENST00000547140.1:n.344A>G
ENST00000547291.1:c.283A>G ENSP00000449838.1:p.Lys95Glu
NM_001946.3:c.658A>G NP_001937.2:p.Lys220Glu
NM_022652.3:c.400+872A>G NP_073143.2:n.400+872A>G
NM_001946.4:c.658A>G MANE Select NP_001937.2:p.Lys220Glu
NM_022652.4:c.400+872A>G NP_073143.2:n.400+872A>G
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