Canonical Allele Identifier: CA1627396946
Gene: MMUT HGNC NCBI

Linked Data

dbSNP Id: rs1767776198

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459279del , CM000668.2:g.49459279del GRCh38
NC_000006.11:g.49426992del , CM000668.1:g.49426992del GRCh37
NC_000006.10:g.49534951del NCBI36
NG_007100.1:g.8864del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.191del MANE Select ENSP00000274813.3:p.Pro64ArgfsTer6
ENST00000274813.3:c.191del ENSP00000274813.3:p.Pro64ArgfsTer6
NM_000255.3:c.191del NP_000246.2:p.Pro64ArgfsTer6
XM_005249143.2:c.191del XP_005249200.1:p.Pro64ArgfsTer6
XM_005249143.3:c.191del XP_005249200.1:p.Pro64ArgfsTer6
NM_000255.4:c.191del MANE Select NP_000246.2:p.Pro64ArgfsTer6