Canonical Allele Identifier: CA341330042
Community Standard Title: NM_001918.5(DBT):c.1232C>T (p.Pro411Leu)
Gene: DBT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100206279G>A , CM000663.2:g.100206279G>A GRCh38
NC_000001.10:g.100671835G>A , CM000663.1:g.100671835G>A GRCh37
NC_000001.9:g.100444423G>A NCBI36
NG_011852.2:g.48575C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001918.5:c.1232C>T MANE Select NP_001909.4:p.Pro411Leu
ENST00000370132.8:c.1232C>T MANE Select ENSP00000359151.3:p.Pro411Leu
NM_001399969.1:c.689C>T NP_001386898.1:p.Pro230Leu
NM_001399972.1:c.689C>T NP_001386901.1:p.Pro230Leu
NM_001918.3:c.1232C>T NP_001909.3:p.Pro411Leu
NM_001918.4:c.1232C>T NP_001909.3:p.Pro411Leu
NR_174363.1:n.1064C>T
NR_174364.1:n.1246C>T
NR_174365.1:n.1029C>T
NR_174366.1:n.1331C>T
ENST00000681617.1:c.1358C>T ENSP00000505544.1:p.Pro453Leu
ENST00000681780.1:c.689C>T ENSP00000505780.1:p.Pro230Leu
XM_005270545.2:c.689C>T XP_005270602.1:p.Pro230Leu
XM_005270545.4:c.689C>T XP_005270602.1:p.Pro230Leu
XM_005270546.2:c.689C>T XP_005270603.1:p.Pro230Leu
XM_017000468.2:c.689C>T XP_016855957.1:p.Pro230Leu
XM_017000469.2:c.689C>T XP_016855958.1:p.Pro230Leu