Canonical Allele Identifier: CA825473993
Gene: MMUT HGNC NCBI

Linked Data

dbSNP Id: rs1208114664
MyVariant Identifiers: chr6:g.49415590_49415591insT (hg19) chr6:g.49447877_49447878insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49447880dup , CM000668.2:g.49447880dup GRCh38
NC_000006.11:g.49415593dup , CM000668.1:g.49415593dup GRCh37
NC_000006.10:g.49523552dup NCBI36
NG_007100.1:g.20262dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1445-93dup MANE Select ENSP00000274813.3:n.1445-93dup
ENST00000274813.3:c.1445-93dup ENSP00000274813.3:n.1445-93dup
NM_000255.3:c.1445-93dup NP_000246.2:n.1445-93dup
XM_005249143.2:c.1445-93dup XP_005249200.1:n.1445-93dup
XM_005249143.3:c.1445-93dup XP_005249200.1:n.1445-93dup
NM_000255.4:c.1445-93dup MANE Select NP_000246.2:n.1445-93dup
Search 100 bp 5'
Search 100 bp 3'