Canonical Allele Identifier: CA385987554
Gene: DUSP6 HGNC NCBI

Linked Data

gnomAD v4: 12-89350773-C-T
MyVariant Identifiers: chr12:g.89744550C>T (hg19) chr12:g.89350773C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.89350773C>T , CM000674.2:g.89350773C>T GRCh38
NC_000012.11:g.89744550C>T , CM000674.1:g.89744550C>T GRCh37
NC_000012.10:g.88268681C>T NCBI36
NG_033915.1:g.7087G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000279488.8:c.653G>A MANE Select ENSP00000279488.6:p.Cys218Tyr
ENST00000279488.7:c.653G>A ENSP00000279488.6:p.Cys218Tyr
ENST00000308385.6:c.400+867G>A ENSP00000307835.6:n.400+867G>A
ENST00000547140.1:n.339G>A
ENST00000547291.1:c.278G>A ENSP00000449838.1:p.Cys93Tyr
NM_001946.3:c.653G>A NP_001937.2:p.Cys218Tyr
NM_022652.3:c.400+867G>A NP_073143.2:n.400+867G>A
NM_001946.4:c.653G>A MANE Select NP_001937.2:p.Cys218Tyr
NM_022652.4:c.400+867G>A NP_073143.2:n.400+867G>A
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