Canonical Allele Identifier: CA2679046365

Gene: MMUT

Linked Data

• gnomAD v4: 6-49447637-T-TAA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49447637_49447638insAA , CM000668.2:g.49447637_49447638insAA	GRCh38
NC_000006.11:g.49415350_49415351insAA , CM000668.1:g.49415350_49415351insAA	GRCh37
NC_000006.10:g.49523309_49523310insAA	NCBI36
NG_007100.1:g.20502_20503insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.1560+32_1560+33insTT MANE Select	ENSP00000274813.3:n.1560+32_1560+33insTT
ENST00000274813.3:c.1560+32_1560+33insTT	ENSP00000274813.3:n.1560+32_1560+33insTT
NM_000255.3:c.1560+32_1560+33insTT	NP_000246.2:n.1560+32_1560+33insTT
XM_005249143.2:c.1560+32_1560+33insTT	XP_005249200.1:n.1560+32_1560+33insTT
XM_005249143.3:c.1560+32_1560+33insTT	XP_005249200.1:n.1560+32_1560+33insTT
NM_000255.4:c.1560+32_1560+33insTT MANE Select	NP_000246.2:n.1560+32_1560+33insTT