Canonical Allele Identifier: CA1627397147
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459402G= , CM000668.2:g.49459402G= GRCh38
NC_000006.11:g.49427115G= , CM000668.1:g.49427115G= GRCh37
NC_000006.10:g.49535074G= NCBI36
NG_007100.1:g.8738C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.65C= MANE Select ENSP00000274813.3:p.Ser22=
ENST00000274813.3:c.65C= ENSP00000274813.3:p.Ser22=
NM_000255.3:c.65C= NP_000246.2:p.Ser22=
XM_005249143.2:c.65C= XP_005249200.1:p.Ser22=
XM_005249143.3:c.65C= XP_005249200.1:p.Ser22=
NM_000255.4:c.65C= MANE Select NP_000246.2:p.Ser22=