Canonical Allele Identifier: CA1627396341

Gene: MMUT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49459038_49459039delinsCA , CM000668.2:g.49459038_49459039delinsCA	GRCh38
NC_000006.11:g.49426751_49426752delinsCA , CM000668.1:g.49426751_49426752delinsCA	GRCh37
NC_000006.10:g.49534710_49534711delinsCA	NCBI36
NG_007100.1:g.9101_9102delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.385+43_385+44delinsTG MANE Select	ENSP00000274813.3:n.385+43_385+44delinsTG
ENST00000274813.3:c.385+43_385+44delinsTG	ENSP00000274813.3:n.385+43_385+44delinsTG
NM_000255.3:c.385+43_385+44delinsTG	NP_000246.2:n.385+43_385+44delinsTG
XM_005249143.2:c.385+43_385+44delinsTG	XP_005249200.1:n.385+43_385+44delinsTG
XM_005249143.3:c.385+43_385+44delinsTG	XP_005249200.1:n.385+43_385+44delinsTG
NM_000255.4:c.385+43_385+44delinsTG MANE Select	NP_000246.2:n.385+43_385+44delinsTG