Canonical Allele Identifier: CA382888406
Gene: HMBS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119088659G>T , CM000673.2:g.119088659G>T GRCh38
NC_000011.9:g.118959369G>T , CM000673.1:g.118959369G>T GRCh37
NC_000011.8:g.118464579G>T NCBI36
NG_008093.1:g.8783G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.-54G>T ENSP00000509288.1:n.-54G>T
ENST00000686690.1:n.274G>T
ENST00000691144.1:n.1394G>T
ENST00000691249.1:n.696G>T
ENST00000442944.7:c.112G>T ENSP00000392041.3:p.Val38Leu
ENST00000534956.2:n.61G>T
ENST00000536813.6:c.61G>T ENSP00000438726.2:p.Val21Leu
ENST00000546302.6:c.112G>T ENSP00000445599.1:p.Val38Leu
ENST00000640813.1:c.61G>T ENSP00000491061.1:p.Val21Leu
ENST00000648026.1:c.106G>T ENSP00000498044.1:p.Val36Leu
ENST00000648374.1:c.61G>T ENSP00000497255.1:p.Val21Leu
ENST00000648488.1:c.61G>T ENSP00000498079.1:p.Val21Leu
ENST00000649823.1:n.329G>T
ENST00000649868.1:c.34-441G>T ENSP00000497548.1:n.34-441G>T
ENST00000650101.1:c.61G>T ENSP00000496970.1:p.Val21Leu
ENST00000650307.1:n.564G>T
ENST00000652429.1:c.112G>T MANE Select ENSP00000498786.1:p.Val38Leu
ENST00000278715.7:c.112G>T ENSP00000278715.3:p.Val38Leu
ENST00000392841.1:c.61G>T ENSP00000376584.1:p.Val21Leu
ENST00000442944.6:c.61G>T ENSP00000392041.2:p.Val21Leu
ENST00000534956.1:n.28G>T
ENST00000535253.5:c.61G>T ENSP00000442079.1:p.Val21Leu
ENST00000535793.5:c.58G>T ENSP00000439904.1:p.Val20Leu
ENST00000536185.5:n.280G>T
ENST00000536813.5:c.112G>T ENSP00000438726.1:p.Val38Leu
ENST00000537841.5:c.61G>T ENSP00000444730.1:p.Val21Leu
ENST00000539986.5:c.61G>T ENSP00000440092.1:p.Val21Leu
ENST00000542044.5:n.183G>T
ENST00000542345.5:n.250G>T
ENST00000542729.5:c.61G>T ENSP00000443058.1:p.Val21Leu
ENST00000542822.5:c.203G>T ENSP00000444817.1:p.Cys68Phe
ENST00000543090.5:c.58G>T ENSP00000445429.1:p.Val20Leu
ENST00000543543.5:n.347G>T
ENST00000543821.5:n.258G>T
ENST00000544360.5:n.80G>T
ENST00000544387.5:c.112G>T ENSP00000438424.1:p.Val38Leu
ENST00000545621.5:c.112G>T ENSP00000444849.1:p.Val38Leu
ENST00000545901.5:n.265G>T
ENST00000546226.5:n.171G>T
ENST00000546302.5:c.112G>T ENSP00000445599.1:p.Val38Leu
NM_000190.3:c.112G>T NP_000181.2:p.Val38Leu
NM_001024382.1:c.61G>T NP_001019553.1:p.Val21Leu
NM_001258208.1:c.112G>T NP_001245137.1:p.Val38Leu
NM_001258209.1:c.61G>T NP_001245138.1:p.Val21Leu
XM_005271531.1:c.61G>T XP_005271588.1:p.Val21Leu
XM_005271532.1:c.61G>T XP_005271589.1:p.Val21Leu
XM_005271533.2:c.58G>T XP_005271590.1:p.Val20Leu
XM_011542796.1:c.-54G>T XP_011541098.1:n.-54G>T
NM_000190.4:c.112G>T MANE Select NP_000181.2:p.Val38Leu
NM_001024382.2:c.61G>T NP_001019553.1:p.Val21Leu
XM_005271533.3:c.58G>T XP_005271590.1:p.Val20Leu
XM_017017629.1:c.61G>T XP_016873118.1:p.Val21Leu
XM_024448460.1:c.58G>T XP_024304228.1:p.Val20Leu
NM_001258208.2:c.112G>T NP_001245137.1:p.Val38Leu
NM_001258209.2:c.61G>T NP_001245138.1:p.Val21Leu