Canonical Allele Identifier: CA2616354660
Gene: HMBS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119092108del , CM000673.2:g.119092108del GRCh38
NC_000011.9:g.118962818del , CM000673.1:g.118962818del GRCh37
NC_000011.8:g.118468028del NCBI36
NG_008093.1:g.12232del

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.448-17del ENSP00000509288.1:n.448-17del
ENST00000691144.1:n.2354-17del
ENST00000691249.1:n.1197-17del
ENST00000442944.7:c.595-17del ENSP00000392041.3:n.595-17del
ENST00000536813.6:c.562-17del ENSP00000438726.2:n.562-17del
ENST00000546302.6:c.535-17del ENSP00000445599.1:n.535-17del
ENST00000640813.1:c.461+234del ENSP00000491061.1:n.461+234del
ENST00000648026.1:c.507-17del ENSP00000498044.1:n.507-17del
ENST00000648374.1:c.562-17del ENSP00000497255.1:n.562-17del
ENST00000648488.1:c.*86-17del ENSP00000498079.1:n.*86-17del
ENST00000649823.1:n.830-17del
ENST00000650101.1:c.544-17del ENSP00000496970.1:n.544-17del
ENST00000650307.1:n.1439-17del
ENST00000652429.1:c.613-17del MANE Select ENSP00000498786.1:n.613-17del
ENST00000278715.7:c.613-17del ENSP00000278715.3:n.613-17del
ENST00000392841.1:c.562-17del ENSP00000376584.1:n.562-17del
ENST00000442944.6:c.562-17del ENSP00000392041.2:n.562-17del
ENST00000537841.5:c.562-17del ENSP00000444730.1:n.562-17del
ENST00000542044.5:n.1058-17del
ENST00000542345.5:n.751-17del
ENST00000542729.5:c.562-17del ENSP00000443058.1:n.562-17del
ENST00000543090.5:c.559-296del ENSP00000445429.1:n.559-296del
ENST00000543543.5:n.848-17del
ENST00000544182.1:n.571del
ENST00000544387.5:c.613-17del ENSP00000438424.1:n.613-17del
ENST00000545621.5:c.*508-17del ENSP00000444849.1:n.*508-17del
ENST00000546226.5:n.901-17del
ENST00000546302.5:c.535-17del ENSP00000445599.1:n.535-17del
NM_000190.3:c.613-17del NP_000181.2:n.613-17del
NM_001024382.1:c.562-17del NP_001019553.1:n.562-17del
NM_001258208.1:c.613-17del NP_001245137.1:n.613-17del
NM_001258209.1:c.562-17del NP_001245138.1:n.562-17del
XM_005271531.1:c.562-17del XP_005271588.1:n.562-17del
XM_005271532.1:c.562-17del XP_005271589.1:n.562-17del
XM_005271533.2:c.559-17del XP_005271590.1:n.559-17del
XM_011542796.1:c.448-17del XP_011541098.1:n.448-17del
NM_000190.4:c.613-17del MANE Select NP_000181.2:n.613-17del
NM_001024382.2:c.562-17del NP_001019553.1:n.562-17del
XM_005271533.3:c.559-17del XP_005271590.1:n.559-17del
XM_017017629.1:c.562-17del XP_016873118.1:n.562-17del
XM_024448460.1:c.559-17del XP_024304228.1:n.559-17del
NM_001258208.2:c.613-17del NP_001245137.1:n.613-17del
NM_001258209.2:c.562-17del NP_001245138.1:n.562-17del