Canonical Allele Identifier: CA1627396231
Gene: MMUT HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49458945C= , CM000668.2:g.49458945C= GRCh38
NC_000006.11:g.49426658C= , CM000668.1:g.49426658C= GRCh37
NC_000006.10:g.49534617C= NCBI36
NG_007100.1:g.9195G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.385+137G= MANE Select ENSP00000274813.3:n.385+137G=
ENST00000274813.3:c.385+137G= ENSP00000274813.3:n.385+137G=
NM_000255.3:c.385+137G= NP_000246.2:n.385+137G=
XM_005249143.2:c.385+137G= XP_005249200.1:n.385+137G=
XM_005249143.3:c.385+137G= XP_005249200.1:n.385+137G=
NM_000255.4:c.385+137G= MANE Select NP_000246.2:n.385+137G=
Search 100 bp 5'
Search 100 bp 3'