Canonical Allele Identifier: CA2512341428
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459164_49459165insAAAGGCTCAAAGCCCGGCAGCGTGTCG , CM000668.2:g.49459164_49459165insAAAGGCTCAAAGCCCGGCAGCGTGTCG GRCh38
NC_000006.11:g.49426877_49426878insAAAGGCTCAAAGCCCGGCAGCGTGTCG , CM000668.1:g.49426877_49426878insAAAGGCTCAAAGCCCGGCAGCGTGTCG GRCh37
NC_000006.10:g.49534836_49534837insAAAGGCTCAAAGCCCGGCAGCGTGTCG NCBI36
NG_007100.1:g.8976_8977insGACACGCTGCCGGGCTTTGAGCCTTTC

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.303_304insGACACGCTGCCGGGCTTTGAGCCTTTC MANE Select ENSP00000274813.3:p.Thr101_Phe102insAspTh...
ENST00000274813.3:c.303_304insGACACGCTGCCGGGCTTTGAGCCTTTC ENSP00000274813.3:p.Thr101_Phe102insAspTh...
NM_000255.3:c.303_304insGACACGCTGCCGGGCTTTGAGCCTTTC NP_000246.2:p.Thr101_Phe102insAspThrLeuPr...
XM_005249143.2:c.303_304insGACACGCTGCCGGGCTTTGAGCCTTTC XP_005249200.1:p.Thr101_Phe102insAspThrLe...
XM_005249143.3:c.303_304insGACACGCTGCCGGGCTTTGAGCCTTTC XP_005249200.1:p.Thr101_Phe102insAspThrLe...
NM_000255.4:c.303_304insGACACGCTGCCGGGCTTTGAGCCTTTC MANE Select NP_000246.2:p.Thr101_Phe102insAspThrLeuPr...