Canonical Allele Identifier: CA1627388080
Gene: MMUT HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49448790A= , CM000668.2:g.49448790A= GRCh38
NC_000006.11:g.49416503A= , CM000668.1:g.49416503A= GRCh37
NC_000006.10:g.49524462A= NCBI36
NG_007100.1:g.19350T=

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.1444+26T= MANE Select ENSP00000274813.3:n.1444+26T=
ENST00000274813.3:c.1444+26T= ENSP00000274813.3:n.1444+26T=
NM_000255.3:c.1444+26T= NP_000246.2:n.1444+26T=
XM_005249143.2:c.1444+26T= XP_005249200.1:n.1444+26T=
XM_005249143.3:c.1444+26T= XP_005249200.1:n.1444+26T=
NM_000255.4:c.1444+26T= MANE Select NP_000246.2:n.1444+26T=
Search 100 bp 5'
Search 100 bp 3'