Canonical Allele Identifier: CA1627396368
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459050_49459052delinsCAT , CM000668.2:g.49459050_49459052delinsCAT GRCh38
NC_000006.11:g.49426763_49426765delinsCAT , CM000668.1:g.49426763_49426765delinsCAT GRCh37
NC_000006.10:g.49534722_49534724delinsCAT NCBI36
NG_007100.1:g.9088_9090delinsATG

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.385+30_385+32delinsATG MANE Select ENSP00000274813.3:n.385+30_385+32delinsAT...
ENST00000274813.3:c.385+30_385+32delinsATG ENSP00000274813.3:n.385+30_385+32delinsAT...
NM_000255.3:c.385+30_385+32delinsATG NP_000246.2:n.385+30_385+32delinsATG
XM_005249143.2:c.385+30_385+32delinsATG XP_005249200.1:n.385+30_385+32delinsATG
XM_005249143.3:c.385+30_385+32delinsATG XP_005249200.1:n.385+30_385+32delinsATG
NM_000255.4:c.385+30_385+32delinsATG MANE Select NP_000246.2:n.385+30_385+32delinsATG