Canonical Allele Identifier: CA2770993484
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49431724G>C , CM000668.2:g.49431724G>C GRCh38
NC_000006.11:g.49399437G>C , CM000668.1:g.49399437G>C GRCh37
NC_000006.10:g.49507396G>C NCBI36
NG_007100.1:g.36416C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.*4C>G MANE Select ENSP00000274813.3:n.*4C>G
ENST00000274813.3:c.*4C>G ENSP00000274813.3:n.*4C>G
NM_000255.3:c.*4C>G NP_000246.2:n.*4C>G
XM_005249143.2:c.*4C>G XP_005249200.1:n.*4C>G
XM_005249143.3:c.*4C>G XP_005249200.1:n.*4C>G
NM_000255.4:c.*4C>G MANE Select NP_000246.2:n.*4C>G