Canonical Allele Identifier: CA1627397577
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459509_49459510delinsGA , CM000668.2:g.49459509_49459510delinsGA GRCh38
NC_000006.11:g.49427222_49427223delinsGA , CM000668.1:g.49427222_49427223delinsGA GRCh37
NC_000006.10:g.49535181_49535182delinsGA NCBI36
NG_007100.1:g.8630_8631delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.-39-5_-39-4delinsTC MANE Select ENSP00000274813.3:n.-39-5_-39-4delinsTC
ENST00000274813.3:c.-39-5_-39-4delinsTC ENSP00000274813.3:n.-39-5_-39-4delinsTC
NM_000255.3:c.-39-5_-39-4delinsTC NP_000246.2:n.-39-5_-39-4delinsTC
XM_005249143.2:c.-39-5_-39-4delinsTC XP_005249200.1:n.-39-5_-39-4delinsTC
XM_005249143.3:c.-39-5_-39-4delinsTC XP_005249200.1:n.-39-5_-39-4delinsTC
NM_000255.4:c.-39-5_-39-4delinsTC MANE Select NP_000246.2:n.-39-5_-39-4delinsTC