Canonical Allele Identifier: CA1627396258

Gene: MMUT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49458975_49458980delinsAAAATT , CM000668.2:g.49458975_49458980delinsAAAATT	GRCh38
NC_000006.11:g.49426688_49426693delinsAAAATT , CM000668.1:g.49426688_49426693delinsAAAATT	GRCh37
NC_000006.10:g.49534647_49534652delinsAAAATT	NCBI36
NG_007100.1:g.9160_9165delinsAATTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000274813.4:c.385+102_385+107delinsAATTTT MANE Select	ENSP00000274813.3:n.385+102_385+107delinsAATTTT
ENST00000274813.3:c.385+102_385+107delinsAATTTT	ENSP00000274813.3:n.385+102_385+107delinsAATTTT
NM_000255.3:c.385+102_385+107delinsAATTTT	NP_000246.2:n.385+102_385+107delinsAATTTT
XM_005249143.2:c.385+102_385+107delinsAATTTT	XP_005249200.1:n.385+102_385+107delinsAATTTT
XM_005249143.3:c.385+102_385+107delinsAATTTT	XP_005249200.1:n.385+102_385+107delinsAATTTT
NM_000255.4:c.385+102_385+107delinsAATTTT MANE Select	NP_000246.2:n.385+102_385+107delinsAATTTT