Canonical Allele Identifier: CA1627396381
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459052_49459053delinsTA , CM000668.2:g.49459052_49459053delinsTA GRCh38
NC_000006.11:g.49426765_49426766delinsTA , CM000668.1:g.49426765_49426766delinsTA GRCh37
NC_000006.10:g.49534724_49534725delinsTA NCBI36
NG_007100.1:g.9087_9088delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.385+29_385+30delinsTA MANE Select ENSP00000274813.3:n.385+29_385+30delinsTA...
ENST00000274813.3:c.385+29_385+30delinsTA ENSP00000274813.3:n.385+29_385+30delinsTA...
NM_000255.3:c.385+29_385+30delinsTA NP_000246.2:n.385+29_385+30delinsTA
XM_005249143.2:c.385+29_385+30delinsTA XP_005249200.1:n.385+29_385+30delinsTA
XM_005249143.3:c.385+29_385+30delinsTA XP_005249200.1:n.385+29_385+30delinsTA
NM_000255.4:c.385+29_385+30delinsTA MANE Select NP_000246.2:n.385+29_385+30delinsTA