Canonical Allele Identifier: CA1627396707
Gene: MMUT HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459183G= , CM000668.2:g.49459183G= GRCh38
NC_000006.11:g.49426896G= , CM000668.1:g.49426896G= GRCh37
NC_000006.10:g.49534855G= NCBI36
NG_007100.1:g.8957C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.284C= MANE Select ENSP00000274813.3:p.Pro95=
ENST00000274813.3:c.284C= ENSP00000274813.3:p.Pro95=
NM_000255.3:c.284C= NP_000246.2:p.Pro95=
XM_005249143.2:c.284C= XP_005249200.1:p.Pro95=
XM_005249143.3:c.284C= XP_005249200.1:p.Pro95=
NM_000255.4:c.284C= MANE Select NP_000246.2:p.Pro95=
Search 100 bp 5'
Search 100 bp 3'