Canonical Allele Identifier: CA1627396316
Gene: MMUT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459023T= , CM000668.2:g.49459023T= GRCh38
NC_000006.11:g.49426736T= , CM000668.1:g.49426736T= GRCh37
NC_000006.10:g.49534695T= NCBI36
NG_007100.1:g.9117A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.385+59A= MANE Select ENSP00000274813.3:n.385+59A=
ENST00000274813.3:c.385+59A= ENSP00000274813.3:n.385+59A=
NM_000255.3:c.385+59A= NP_000246.2:n.385+59A=
XM_005249143.2:c.385+59A= XP_005249200.1:n.385+59A=
XM_005249143.3:c.385+59A= XP_005249200.1:n.385+59A=
NM_000255.4:c.385+59A= MANE Select NP_000246.2:n.385+59A=
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