Canonical Allele Identifier: CA1627387564

Gene: MMUT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49447597_49447598delinsAG , CM000668.2:g.49447597_49447598delinsAG	GRCh38
NC_000006.11:g.49415310_49415311delinsAG , CM000668.1:g.49415310_49415311delinsAG	GRCh37
NC_000006.10:g.49523269_49523270delinsAG	NCBI36
NG_007100.1:g.20542_20543delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.1560+72_1560+73delinsCT MANE Select	ENSP00000274813.3:n.1560+72_1560+73delinsCT
ENST00000274813.3:c.1560+72_1560+73delinsCT	ENSP00000274813.3:n.1560+72_1560+73delinsCT
NM_000255.3:c.1560+72_1560+73delinsCT	NP_000246.2:n.1560+72_1560+73delinsCT
XM_005249143.2:c.1560+72_1560+73delinsCT	XP_005249200.1:n.1560+72_1560+73delinsCT
XM_005249143.3:c.1560+72_1560+73delinsCT	XP_005249200.1:n.1560+72_1560+73delinsCT
NM_000255.4:c.1560+72_1560+73delinsCT MANE Select	NP_000246.2:n.1560+72_1560+73delinsCT