Canonical Allele Identifier: CA364404876
Gene: MMUT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459092G>T , CM000668.2:g.49459092G>T GRCh38
NC_000006.11:g.49426805G>T , CM000668.1:g.49426805G>T GRCh37
NC_000006.10:g.49534764G>T NCBI36
NG_007100.1:g.9048C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.375C>A MANE Select ENSP00000274813.3:p.Asp125Glu
ENST00000274813.3:c.375C>A ENSP00000274813.3:p.Asp125Glu
NM_000255.3:c.375C>A NP_000246.2:p.Asp125Glu
XM_005249143.2:c.375C>A XP_005249200.1:p.Asp125Glu
XM_005249143.3:c.375C>A XP_005249200.1:p.Asp125Glu
NM_000255.4:c.375C>A MANE Select NP_000246.2:p.Asp125Glu