Canonical Allele Identifier: CA341329753
Community Standard Title: NM_001918.5(DBT):c.1274C>G (p.Ser425Ter)
Gene: DBT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100206237G>C , CM000663.2:g.100206237G>C GRCh38
NC_000001.10:g.100671793G>C , CM000663.1:g.100671793G>C GRCh37
NC_000001.9:g.100444381G>C NCBI36
NG_011852.2:g.48617C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001918.5:c.1274C>G MANE Select NP_001909.4:p.Ser425Ter
ENST00000370132.8:c.1274C>G MANE Select ENSP00000359151.3:p.Ser425Ter
NM_001399969.1:c.731C>G NP_001386898.1:p.Ser244Ter
NM_001399972.1:c.731C>G NP_001386901.1:p.Ser244Ter
NM_001918.3:c.1274C>G NP_001909.3:p.Ser425Ter
NM_001918.4:c.1274C>G NP_001909.3:p.Ser425Ter
NR_174363.1:n.1106C>G
NR_174364.1:n.1288C>G
NR_174365.1:n.1071C>G
NR_174366.1:n.1373C>G
ENST00000681617.1:c.1400C>G ENSP00000505544.1:p.Ser467Ter
ENST00000681780.1:c.731C>G ENSP00000505780.1:p.Ser244Ter
XM_005270545.2:c.731C>G XP_005270602.1:p.Ser244Ter
XM_005270545.4:c.731C>G XP_005270602.1:p.Ser244Ter
XM_005270546.2:c.731C>G XP_005270603.1:p.Ser244Ter
XM_017000468.2:c.731C>G XP_016855957.1:p.Ser244Ter
XM_017000469.2:c.731C>G XP_016855958.1:p.Ser244Ter