Canonical Allele Identifier: CA1627387681

Gene: MMUT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49447847_49447850delinsTATG , CM000668.2:g.49447847_49447850delinsTATG	GRCh38
NC_000006.11:g.49415560_49415563delinsTATG , CM000668.1:g.49415560_49415563delinsTATG	GRCh37
NC_000006.10:g.49523519_49523522delinsTATG	NCBI36
NG_007100.1:g.20290_20293delinsCATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.1445-65_1445-62delinsCATA MANE Select	ENSP00000274813.3:n.1445-65_1445-62delinsCATA
ENST00000274813.3:c.1445-65_1445-62delinsCATA	ENSP00000274813.3:n.1445-65_1445-62delinsCATA
NM_000255.3:c.1445-65_1445-62delinsCATA	NP_000246.2:n.1445-65_1445-62delinsCATA
XM_005249143.2:c.1445-65_1445-62delinsCATA	XP_005249200.1:n.1445-65_1445-62delinsCATA
XM_005249143.3:c.1445-65_1445-62delinsCATA	XP_005249200.1:n.1445-65_1445-62delinsCATA
NM_000255.4:c.1445-65_1445-62delinsCATA MANE Select	NP_000246.2:n.1445-65_1445-62delinsCATA