Canonical Allele Identifier: CA1627387590
Gene: MMUT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49447644A= , CM000668.2:g.49447644A= GRCh38
NC_000006.11:g.49415357A= , CM000668.1:g.49415357A= GRCh37
NC_000006.10:g.49523316A= NCBI36
NG_007100.1:g.20496T=

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.1560+26T= MANE Select ENSP00000274813.3:n.1560+26T=
ENST00000274813.3:c.1560+26T= ENSP00000274813.3:n.1560+26T=
NM_000255.3:c.1560+26T= NP_000246.2:n.1560+26T=
XM_005249143.2:c.1560+26T= XP_005249200.1:n.1560+26T=
XM_005249143.3:c.1560+26T= XP_005249200.1:n.1560+26T=
NM_000255.4:c.1560+26T= MANE Select NP_000246.2:n.1560+26T=
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