Canonical Allele Identifier: CA1627397513
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459501C= , CM000668.2:g.49459501C= GRCh38
NC_000006.11:g.49427214C= , CM000668.1:g.49427214C= GRCh37
NC_000006.10:g.49535173C= NCBI36
NG_007100.1:g.8639G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.-35G= MANE Select ENSP00000274813.3:n.-35G=
ENST00000274813.3:c.-35G= ENSP00000274813.3:n.-35G=
NM_000255.3:c.-35G= NP_000246.2:n.-35G=
XM_005249143.2:c.-35G= XP_005249200.1:n.-35G=
XM_005249143.3:c.-35G= XP_005249200.1:n.-35G=
NM_000255.4:c.-35G= MANE Select NP_000246.2:n.-35G=