Canonical Allele Identifier: CA1627386264

Gene: MMUT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49444495_49444498delinsTAAG , CM000668.2:g.49444495_49444498delinsTAAG	GRCh38
NC_000006.11:g.49412208_49412211delinsTAAG , CM000668.1:g.49412208_49412211delinsTAAG	GRCh37
NC_000006.10:g.49520167_49520170delinsTAAG	NCBI36
NG_007100.1:g.23642_23645delinsCTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.1676+141_1676+144delinsCTTA MANE Select	ENSP00000274813.3:n.1676+141_1676+144delinsCTTA
ENST00000274813.3:c.1676+141_1676+144delinsCTTA	ENSP00000274813.3:n.1676+141_1676+144delinsCTTA
NM_000255.3:c.1676+141_1676+144delinsCTTA	NP_000246.2:n.1676+141_1676+144delinsCTTA
XM_005249143.2:c.1676+141_1676+144delinsCTTA	XP_005249200.1:n.1676+141_1676+144delinsCTTA
XM_005249143.3:c.1676+141_1676+144delinsCTTA	XP_005249200.1:n.1676+141_1676+144delinsCTTA
NM_000255.4:c.1676+141_1676+144delinsCTTA MANE Select	NP_000246.2:n.1676+141_1676+144delinsCTTA