Canonical Allele Identifier: CA2711790810
Gene: MMUT HGNC NCBI

Linked Data

dbSNP Id: rs2127416773
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49447646_49447647insCAA , CM000668.2:g.49447646_49447647insCAA GRCh38
NC_000006.11:g.49415359_49415360insCAA , CM000668.1:g.49415359_49415360insCAA GRCh37
NC_000006.10:g.49523318_49523319insCAA NCBI36
NG_007100.1:g.20495_20496insGTT

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.1560+25_1560+26insGTT MANE Select ENSP00000274813.3:n.1560+25_1560+26insGTT...
ENST00000274813.3:c.1560+25_1560+26insGTT ENSP00000274813.3:n.1560+25_1560+26insGTT...
NM_000255.3:c.1560+25_1560+26insGTT NP_000246.2:n.1560+25_1560+26insGTT
XM_005249143.2:c.1560+25_1560+26insGTT XP_005249200.1:n.1560+25_1560+26insGTT
XM_005249143.3:c.1560+25_1560+26insGTT XP_005249200.1:n.1560+25_1560+26insGTT
NM_000255.4:c.1560+25_1560+26insGTT MANE Select NP_000246.2:n.1560+25_1560+26insGTT
Search 100 bp 5'
Search 100 bp 3'