Canonical Allele Identifier: CA481304484

Gene: DUSP6

Linked Data

• MyVariant Identifiers: chr12:g.89744630T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.89350853T>A , CM000674.2:g.89350853T>A	GRCh38
NC_000012.11:g.89744630T>A , CM000674.1:g.89744630T>A	GRCh37
NC_000012.10:g.88268761T>A	NCBI36
NG_033915.1:g.7007A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279488.8:c.573A>T MANE Select	ENSP00000279488.6:p.Ala191=
ENST00000279488.7:c.573A>T	ENSP00000279488.6:p.Ala191=
ENST00000308385.6:c.400+787A>T	ENSP00000307835.6:n.400+787A>T
ENST00000547140.1:n.259A>T
ENST00000547291.1:c.198A>T	ENSP00000449838.1:p.Ala66=
NM_001946.3:c.573A>T	NP_001937.2:p.Ala191=
NM_022652.3:c.400+787A>T	NP_073143.2:n.400+787A>T
NM_001946.4:c.573A>T MANE Select	NP_001937.2:p.Ala191=
NM_022652.4:c.400+787A>T	NP_073143.2:n.400+787A>T