Canonical Allele Identifier: CA825473782
Gene: MMUT HGNC NCBI

Linked Data

dbSNP Id: rs1436881074
gnomAD v3: 6-49447847-TATG-T
gnomAD v4: 6-49447847-TATG-T
MyVariant Identifiers: chr6:g.49415561_49415563del (hg19) chr6:g.49447848_49447850del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49447851_49447853del , CM000668.2:g.49447851_49447853del GRCh38
NC_000006.11:g.49415564_49415566del , CM000668.1:g.49415564_49415566del GRCh37
NC_000006.10:g.49523523_49523525del NCBI36
NG_007100.1:g.20290_20292del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1445-65_1445-63del MANE Select ENSP00000274813.3:n.1445-65_1445-63del
ENST00000274813.3:c.1445-65_1445-63del ENSP00000274813.3:n.1445-65_1445-63del
NM_000255.3:c.1445-65_1445-63del NP_000246.2:n.1445-65_1445-63del
XM_005249143.2:c.1445-65_1445-63del XP_005249200.1:n.1445-65_1445-63del
XM_005249143.3:c.1445-65_1445-63del XP_005249200.1:n.1445-65_1445-63del
NM_000255.4:c.1445-65_1445-63del MANE Select NP_000246.2:n.1445-65_1445-63del
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