Canonical Allele Identifier: CA364399038

Gene: MMUT

Linked Data

• MyVariant Identifiers: chr6:g.49419373C>A (hg19) ; chr6:g.49451660C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49451660C>A , CM000668.2:g.49451660C>A	GRCh38
NC_000006.11:g.49419373C>A , CM000668.1:g.49419373C>A	GRCh37
NC_000006.10:g.49527332C>A	NCBI36
NG_007100.1:g.16480G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.1138G>T MANE Select	ENSP00000274813.3:p.Gly380Ter
ENST00000274813.3:c.1138G>T	ENSP00000274813.3:p.Gly380Ter
NM_000255.3:c.1138G>T	NP_000246.2:p.Gly380Ter
XM_005249143.2:c.1138G>T	XP_005249200.1:p.Gly380Ter
XM_005249143.3:c.1138G>T	XP_005249200.1:p.Gly380Ter
NM_000255.4:c.1138G>T MANE Select	NP_000246.2:p.Gly380Ter