Canonical Allele Identifier: CA1627388072
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49448767T= , CM000668.2:g.49448767T= GRCh38
NC_000006.11:g.49416480T= , CM000668.1:g.49416480T= GRCh37
NC_000006.10:g.49524439T= NCBI36
NG_007100.1:g.19373A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1444+49A= MANE Select ENSP00000274813.3:n.1444+49A=
ENST00000274813.3:c.1444+49A= ENSP00000274813.3:n.1444+49A=
NM_000255.3:c.1444+49A= NP_000246.2:n.1444+49A=
XM_005249143.2:c.1444+49A= XP_005249200.1:n.1444+49A=
XM_005249143.3:c.1444+49A= XP_005249200.1:n.1444+49A=
NM_000255.4:c.1444+49A= MANE Select NP_000246.2:n.1444+49A=