Canonical Allele Identifier: CA1184058806

Gene: DBT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100206135_100206136delinsCA , CM000663.2:g.100206135_100206136delinsCA	GRCh38
NC_000001.10:g.100671691_100671692delinsCA , CM000663.1:g.100671691_100671692delinsCA	GRCh37
NC_000001.9:g.100444279_100444280delinsCA	NCBI36
NG_011852.2:g.48718_48719delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681617.1:c.1407+94_1407+95delinsTG	ENSP00000505544.1:n.1407+94_1407+95delinsTG
ENST00000681780.1:c.738+94_738+95delinsTG	ENSP00000505780.1:n.738+94_738+95delinsTG
ENST00000370132.8:c.1281+94_1281+95delinsTG MANE Select	ENSP00000359151.3:n.1281+94_1281+95delinsTG
NM_001918.3:c.1281+94_1281+95delinsTG	NP_001909.3:n.1281+94_1281+95delinsTG
XM_005270545.2:c.738+94_738+95delinsTG	XP_005270602.1:n.738+94_738+95delinsTG
XM_005270546.2:c.738+94_738+95delinsTG	XP_005270603.1:n.738+94_738+95delinsTG
XM_005270545.4:c.738+94_738+95delinsTG	XP_005270602.1:n.738+94_738+95delinsTG
XM_017000468.2:c.738+94_738+95delinsTG	XP_016855957.1:n.738+94_738+95delinsTG
XM_017000469.2:c.738+94_738+95delinsTG	XP_016855958.1:n.738+94_738+95delinsTG
NM_001918.4:c.1281+94_1281+95delinsTG	NP_001909.3:n.1281+94_1281+95delinsTG
NM_001918.5:c.1281+94_1281+95delinsTG MANE Select	NP_001909.4:n.1281+94_1281+95delinsTG
NM_001399969.1:c.738+94_738+95delinsTG	NP_001386898.1:n.738+94_738+95delinsTG
NM_001399972.1:c.738+94_738+95delinsTG	NP_001386901.1:n.738+94_738+95delinsTG
NR_174363.1:n.1113+94_1113+95delinsTG
NR_174364.1:n.1295+94_1295+95delinsTG
NR_174365.1:n.1078+94_1078+95delinsTG
NR_174366.1:n.1380+94_1380+95delinsTG