Canonical Allele Identifier: CA1627389369

Gene: MMUT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49451683_49451706delinsATTGCAGTACGGACAATATTATTG , CM000668.2:g.49451683_49451706delinsATTGCAGTACGGACAATATTATTG	GRCh38
NC_000006.11:g.49419396_49419419delinsATTGCAGTACGGACAATATTATTG , CM000668.1:g.49419396_49419419delinsATTGCAGTACGGACAATATTATTG	GRCh37
NC_000006.10:g.49527355_49527378delinsATTGCAGTACGGACAATATTATTG	NCBI36
NG_007100.1:g.16434_16457delinsCAATAATATTGTCCGTACTGCAAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000274813.4:c.1092_1115delinsCAATAATATTGTCCGTACTGCAAT MANE Select	ENSP00000274813.3:p.Tyr364=
ENST00000274813.3:c.1092_1115delinsCAATAATATTGTCCGTACTGCAAT	ENSP00000274813.3:p.Tyr364=
NM_000255.3:c.1092_1115delinsCAATAATATTGTCCGTACTGCAAT	NP_000246.2:p.Tyr364=
XM_005249143.2:c.1092_1115delinsCAATAATATTGTCCGTACTGCAAT	XP_005249200.1:p.Tyr364=
XM_005249143.3:c.1092_1115delinsCAATAATATTGTCCGTACTGCAAT	XP_005249200.1:p.Tyr364=
NM_000255.4:c.1092_1115delinsCAATAATATTGTCCGTACTGCAAT MANE Select	NP_000246.2:p.Tyr364=