Canonical Allele Identifier: CA450606394

Gene: MMUT

Linked Data

• MyVariant Identifiers: chr6:g.49419281G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49451568G>A , CM000668.2:g.49451568G>A	GRCh38
NC_000006.11:g.49419281G>A , CM000668.1:g.49419281G>A	GRCh37
NC_000006.10:g.49527240G>A	NCBI36
NG_007100.1:g.16572C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.1230C>T MANE Select	ENSP00000274813.3:p.Ile410=
ENST00000274813.3:c.1230C>T	ENSP00000274813.3:p.Ile410=
NM_000255.3:c.1230C>T	NP_000246.2:p.Ile410=
XM_005249143.2:c.1230C>T	XP_005249200.1:p.Ile410=
XM_005249143.3:c.1230C>T	XP_005249200.1:p.Ile410=
NM_000255.4:c.1230C>T MANE Select	NP_000246.2:p.Ile410=