Canonical Allele Identifier: CA2578675217
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49458125T>A , CM000668.2:g.49458125T>A GRCh38
NC_000006.11:g.49425838T>A , CM000668.1:g.49425838T>A GRCh37
NC_000006.10:g.49533797T>A NCBI36
NG_007100.1:g.10015A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.386-67A>T MANE Select ENSP00000274813.3:n.386-67A>T
ENST00000274813.3:c.386-67A>T ENSP00000274813.3:n.386-67A>T
NM_000255.3:c.386-67A>T NP_000246.2:n.386-67A>T
XM_005249143.2:c.386-67A>T XP_005249200.1:n.386-67A>T
XM_005249143.3:c.386-67A>T XP_005249200.1:n.386-67A>T
NM_000255.4:c.386-67A>T MANE Select NP_000246.2:n.386-67A>T