Canonical Allele Identifier: CA2553134313
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459498G>A , CM000668.2:g.49459498G>A GRCh38
NC_000006.11:g.49427211G>A , CM000668.1:g.49427211G>A GRCh37
NC_000006.10:g.49535170G>A NCBI36
NG_007100.1:g.8642C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.-32C>T MANE Select ENSP00000274813.3:n.-32C>T
ENST00000274813.3:c.-32C>T ENSP00000274813.3:n.-32C>T
NM_000255.3:c.-32C>T NP_000246.2:n.-32C>T
XM_005249143.2:c.-32C>T XP_005249200.1:n.-32C>T
XM_005249143.3:c.-32C>T XP_005249200.1:n.-32C>T
NM_000255.4:c.-32C>T MANE Select NP_000246.2:n.-32C>T