Canonical Allele Identifier: CA1088813257

Gene: MMUT

Linked Data

• dbSNP Id: rs1767742184
• gnomAD v3: 6-49458140-T-TA
• gnomAD v4: 6-49458140-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49458140_49458141insA , CM000668.2:g.49458140_49458141insA	GRCh38
NC_000006.11:g.49425853_49425854insA , CM000668.1:g.49425853_49425854insA	GRCh37
NC_000006.10:g.49533812_49533813insA	NCBI36
NG_007100.1:g.9999_10000insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.386-83_386-82insT MANE Select	ENSP00000274813.3:n.386-83_386-82insT
ENST00000274813.3:c.386-83_386-82insT	ENSP00000274813.3:n.386-83_386-82insT
NM_000255.3:c.386-83_386-82insT	NP_000246.2:n.386-83_386-82insT
XM_005249143.2:c.386-83_386-82insT	XP_005249200.1:n.386-83_386-82insT
XM_005249143.3:c.386-83_386-82insT	XP_005249200.1:n.386-83_386-82insT
NM_000255.4:c.386-83_386-82insT MANE Select	NP_000246.2:n.386-83_386-82insT