Canonical Allele Identifier: CA385987495
Gene: DUSP6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.89350767T>G , CM000674.2:g.89350767T>G GRCh38
NC_000012.11:g.89744544T>G , CM000674.1:g.89744544T>G GRCh37
NC_000012.10:g.88268675T>G NCBI36
NG_033915.1:g.7093A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000279488.8:c.659A>C MANE Select ENSP00000279488.6:p.Lys220Thr
ENST00000279488.7:c.659A>C ENSP00000279488.6:p.Lys220Thr
ENST00000308385.6:c.400+873A>C ENSP00000307835.6:n.400+873A>C
ENST00000547140.1:n.345A>C
ENST00000547291.1:c.284A>C ENSP00000449838.1:p.Lys95Thr
NM_001946.3:c.659A>C NP_001937.2:p.Lys220Thr
NM_022652.3:c.400+873A>C NP_073143.2:n.400+873A>C
NM_001946.4:c.659A>C MANE Select NP_001937.2:p.Lys220Thr
NM_022652.4:c.400+873A>C NP_073143.2:n.400+873A>C