Canonical Allele Identifier: CA1627396936
Gene: MMUT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459275_49459276delinsCG , CM000668.2:g.49459275_49459276delinsCG GRCh38
NC_000006.11:g.49426988_49426989delinsCG , CM000668.1:g.49426988_49426989delinsCG GRCh37
NC_000006.10:g.49534947_49534948delinsCG NCBI36
NG_007100.1:g.8864_8865delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.191_192delinsCG MANE Select ENSP00000274813.3:p.Pro64=
ENST00000274813.3:c.191_192delinsCG ENSP00000274813.3:p.Pro64=
NM_000255.3:c.191_192delinsCG NP_000246.2:p.Pro64=
XM_005249143.2:c.191_192delinsCG XP_005249200.1:p.Pro64=
XM_005249143.3:c.191_192delinsCG XP_005249200.1:p.Pro64=
NM_000255.4:c.191_192delinsCG MANE Select NP_000246.2:p.Pro64=
Search 100 bp 5'
Search 100 bp 3'