Canonical Allele Identifier: CA364397298
Gene: MMUT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49447776A>T , CM000668.2:g.49447776A>T GRCh38
NC_000006.11:g.49415489A>T , CM000668.1:g.49415489A>T GRCh37
NC_000006.10:g.49523448A>T NCBI36
NG_007100.1:g.20364T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1454T>A MANE Select ENSP00000274813.3:p.Val485Glu
ENST00000274813.3:c.1454T>A ENSP00000274813.3:p.Val485Glu
NM_000255.3:c.1454T>A NP_000246.2:p.Val485Glu
XM_005249143.2:c.1454T>A XP_005249200.1:p.Val485Glu
XM_005249143.3:c.1454T>A XP_005249200.1:p.Val485Glu
NM_000255.4:c.1454T>A MANE Select NP_000246.2:p.Val485Glu