Canonical Allele Identifier: CA2679046388
Gene: MMUT HGNC NCBI

Linked Data

gnomAD v4: 6-49447654-A-AAT
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49447654_49447655insAT , CM000668.2:g.49447654_49447655insAT GRCh38
NC_000006.11:g.49415367_49415368insAT , CM000668.1:g.49415367_49415368insAT GRCh37
NC_000006.10:g.49523326_49523327insAT NCBI36
NG_007100.1:g.20485_20486insAT

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.1560+15_1560+16insAT MANE Select ENSP00000274813.3:n.1560+15_1560+16insAT
ENST00000274813.3:c.1560+15_1560+16insAT ENSP00000274813.3:n.1560+15_1560+16insAT
NM_000255.3:c.1560+15_1560+16insAT NP_000246.2:n.1560+15_1560+16insAT
XM_005249143.2:c.1560+15_1560+16insAT XP_005249200.1:n.1560+15_1560+16insAT
XM_005249143.3:c.1560+15_1560+16insAT XP_005249200.1:n.1560+15_1560+16insAT
NM_000255.4:c.1560+15_1560+16insAT MANE Select NP_000246.2:n.1560+15_1560+16insAT
Search 100 bp 5'
Search 100 bp 3'