Canonical Allele Identifier: CA2053496147
Gene: DUSP6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.89350779A= , CM000674.2:g.89350779A= GRCh38
NC_000012.11:g.89744556A= , CM000674.1:g.89744556A= GRCh37
NC_000012.10:g.88268687A= NCBI36
NG_033915.1:g.7081T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279488.8:c.647T= MANE Select ENSP00000279488.6:p.Leu216=
ENST00000279488.7:c.647T= ENSP00000279488.6:p.Leu216=
ENST00000308385.6:c.400+861T= ENSP00000307835.6:n.400+861T=
ENST00000547140.1:n.333T=
ENST00000547291.1:c.272T= ENSP00000449838.1:p.Leu91=
NM_001946.3:c.647T= NP_001937.2:p.Leu216=
NM_022652.3:c.400+861T= NP_073143.2:n.400+861T=
NM_001946.4:c.647T= MANE Select NP_001937.2:p.Leu216=
NM_022652.4:c.400+861T= NP_073143.2:n.400+861T=