Canonical Allele Identifier: CA1627386253
Gene: MMUT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49444469T= , CM000668.2:g.49444469T= GRCh38
NC_000006.11:g.49412182T= , CM000668.1:g.49412182T= GRCh37
NC_000006.10:g.49520141T= NCBI36
NG_007100.1:g.23671A=

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.1676+170A= MANE Select ENSP00000274813.3:n.1676+170A=
ENST00000274813.3:c.1676+170A= ENSP00000274813.3:n.1676+170A=
NM_000255.3:c.1676+170A= NP_000246.2:n.1676+170A=
XM_005249143.2:c.1676+170A= XP_005249200.1:n.1676+170A=
XM_005249143.3:c.1676+170A= XP_005249200.1:n.1676+170A=
NM_000255.4:c.1676+170A= MANE Select NP_000246.2:n.1676+170A=
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