Canonical Allele Identifier: CA1627396325

Gene: MMUT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49459035_49459036delinsAG , CM000668.2:g.49459035_49459036delinsAG	GRCh38
NC_000006.11:g.49426748_49426749delinsAG , CM000668.1:g.49426748_49426749delinsAG	GRCh37
NC_000006.10:g.49534707_49534708delinsAG	NCBI36
NG_007100.1:g.9104_9105delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.385+46_385+47delinsCT MANE Select	ENSP00000274813.3:n.385+46_385+47delinsCT
ENST00000274813.3:c.385+46_385+47delinsCT	ENSP00000274813.3:n.385+46_385+47delinsCT
NM_000255.3:c.385+46_385+47delinsCT	NP_000246.2:n.385+46_385+47delinsCT
XM_005249143.2:c.385+46_385+47delinsCT	XP_005249200.1:n.385+46_385+47delinsCT
XM_005249143.3:c.385+46_385+47delinsCT	XP_005249200.1:n.385+46_385+47delinsCT
NM_000255.4:c.385+46_385+47delinsCT MANE Select	NP_000246.2:n.385+46_385+47delinsCT