Canonical Allele Identifier: CA481304435
Gene: DUSP6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.89744582T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.89350805T>G , CM000674.2:g.89350805T>G GRCh38
NC_000012.11:g.89744582T>G , CM000674.1:g.89744582T>G GRCh37
NC_000012.10:g.88268713T>G NCBI36
NG_033915.1:g.7055A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000279488.8:c.621A>C MANE Select ENSP00000279488.6:p.Pro207=
ENST00000279488.7:c.621A>C ENSP00000279488.6:p.Pro207=
ENST00000308385.6:c.400+835A>C ENSP00000307835.6:n.400+835A>C
ENST00000547140.1:n.307A>C
ENST00000547291.1:c.246A>C ENSP00000449838.1:p.Pro82=
NM_001946.3:c.621A>C NP_001937.2:p.Pro207=
NM_022652.3:c.400+835A>C NP_073143.2:n.400+835A>C
NM_001946.4:c.621A>C MANE Select NP_001937.2:p.Pro207=
NM_022652.4:c.400+835A>C NP_073143.2:n.400+835A>C
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