Canonical Allele Identifier: CA1004973968
Gene: DBT HGNC NCBI

Linked Data

dbSNP Id: rs35150096

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100206085_100206090dup , CM000663.2:g.100206085_100206090dup GRCh38
NC_000001.10:g.100671641_100671646dup , CM000663.1:g.100671641_100671646dup GRCh37
NC_000001.9:g.100444229_100444234dup NCBI36
NG_011852.2:g.48776_48781dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000681617.1:c.1407+152_1407+157dup ENSP00000505544.1:n.1407+152_1407+157dup
ENST00000681780.1:c.738+152_738+157dup ENSP00000505780.1:n.738+152_738+157dup
ENST00000370132.8:c.1281+152_1281+157dup MANE Select ENSP00000359151.3:n.1281+152_1281+157dup
NM_001918.3:c.1281+152_1281+157dup NP_001909.3:n.1281+152_1281+157dup
XM_005270545.2:c.738+152_738+157dup XP_005270602.1:n.738+152_738+157dup
XM_005270546.2:c.738+152_738+157dup XP_005270603.1:n.738+152_738+157dup
XM_005270545.4:c.738+152_738+157dup XP_005270602.1:n.738+152_738+157dup
XM_017000468.2:c.738+152_738+157dup XP_016855957.1:n.738+152_738+157dup
XM_017000469.2:c.738+152_738+157dup XP_016855958.1:n.738+152_738+157dup
NM_001918.4:c.1281+152_1281+157dup NP_001909.3:n.1281+152_1281+157dup
NM_001918.5:c.1281+152_1281+157dup MANE Select NP_001909.4:n.1281+152_1281+157dup
NM_001399969.1:c.738+152_738+157dup NP_001386898.1:n.738+152_738+157dup
NM_001399972.1:c.738+152_738+157dup NP_001386901.1:n.738+152_738+157dup
NR_174363.1:n.1113+152_1113+157dup
NR_174364.1:n.1295+152_1295+157dup
NR_174365.1:n.1078+152_1078+157dup
NR_174366.1:n.1380+152_1380+157dup