Canonical Allele Identifier: CA1627396919
Gene: MMUT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459268_49459269delinsTC , CM000668.2:g.49459268_49459269delinsTC GRCh38
NC_000006.11:g.49426981_49426982delinsTC , CM000668.1:g.49426981_49426982delinsTC GRCh37
NC_000006.10:g.49534940_49534941delinsTC NCBI36
NG_007100.1:g.8871_8872delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.198_199delinsGA MANE Select ENSP00000274813.3:p.Gly66=
ENST00000274813.3:c.198_199delinsGA ENSP00000274813.3:p.Gly66=
NM_000255.3:c.198_199delinsGA NP_000246.2:p.Gly66=
XM_005249143.2:c.198_199delinsGA XP_005249200.1:p.Gly66=
XM_005249143.3:c.198_199delinsGA XP_005249200.1:p.Gly66=
NM_000255.4:c.198_199delinsGA MANE Select NP_000246.2:p.Gly66=
Search 100 bp 5'
Search 100 bp 3'