Canonical Allele Identifier: CA1627396386

Gene: MMUT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49459054_49459059delinsAATATT , CM000668.2:g.49459054_49459059delinsAATATT	GRCh38
NC_000006.11:g.49426767_49426772delinsAATATT , CM000668.1:g.49426767_49426772delinsAATATT	GRCh37
NC_000006.10:g.49534726_49534731delinsAATATT	NCBI36
NG_007100.1:g.9081_9086delinsAATATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.385+23_385+28delinsAATATT MANE Select	ENSP00000274813.3:n.385+23_385+28delinsAATATT
ENST00000274813.3:c.385+23_385+28delinsAATATT	ENSP00000274813.3:n.385+23_385+28delinsAATATT
NM_000255.3:c.385+23_385+28delinsAATATT	NP_000246.2:n.385+23_385+28delinsAATATT
XM_005249143.2:c.385+23_385+28delinsAATATT	XP_005249200.1:n.385+23_385+28delinsAATATT
XM_005249143.3:c.385+23_385+28delinsAATATT	XP_005249200.1:n.385+23_385+28delinsAATATT
NM_000255.4:c.385+23_385+28delinsAATATT MANE Select	NP_000246.2:n.385+23_385+28delinsAATATT