Canonical Allele Identifier: CA1627387595

Gene: MMUT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49447654_49447655delinsAG , CM000668.2:g.49447654_49447655delinsAG	GRCh38
NC_000006.11:g.49415367_49415368delinsAG , CM000668.1:g.49415367_49415368delinsAG	GRCh37
NC_000006.10:g.49523326_49523327delinsAG	NCBI36
NG_007100.1:g.20485_20486delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000274813.4:c.1560+15_1560+16delinsCT MANE Select	ENSP00000274813.3:n.1560+15_1560+16delinsCT
ENST00000274813.3:c.1560+15_1560+16delinsCT	ENSP00000274813.3:n.1560+15_1560+16delinsCT
NM_000255.3:c.1560+15_1560+16delinsCT	NP_000246.2:n.1560+15_1560+16delinsCT
XM_005249143.2:c.1560+15_1560+16delinsCT	XP_005249200.1:n.1560+15_1560+16delinsCT
XM_005249143.3:c.1560+15_1560+16delinsCT	XP_005249200.1:n.1560+15_1560+16delinsCT
NM_000255.4:c.1560+15_1560+16delinsCT MANE Select	NP_000246.2:n.1560+15_1560+16delinsCT