Canonical Allele Identifier: CA2003793799
Gene: HMBS HGNC NCBI

Linked Data

dbSNP Id: rs1946334166

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119093382_119093385dup , CM000673.2:g.119093382_119093385dup GRCh38
NC_000011.9:g.118964092_118964095dup , CM000673.1:g.118964092_118964095dup GRCh37
NC_000011.8:g.118469302_118469305dup NCBI36
NG_008093.1:g.13506_13509dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000686218.1:c.*99_*102dup ENSP00000509288.1:n.*99_*102dup
ENST00000691144.1:n.3400_3403dup
ENST00000691249.1:n.2009_2012dup
ENST00000442944.7:c.*99_*102dup ENSP00000392041.3:n.*99_*102dup
ENST00000640813.1:c.*422_*425dup ENSP00000491061.1:n.*422_*425dup
ENST00000648026.1:c.1079_1082dup ENSP00000498044.1:n.1079_1082dup
ENST00000648374.1:c.*99_*102dup ENSP00000497255.1:n.*99_*102dup
ENST00000650101.1:c.*99_*102dup ENSP00000496970.1:n.*99_*102dup
ENST00000650307.1:n.2011_2014dup
ENST00000652429.1:c.*99_*102dup MANE Select ENSP00000498786.1:n.*99_*102dup
ENST00000278715.7:c.*99_*102dup ENSP00000278715.3:n.*99_*102dup
ENST00000392841.1:c.*99_*102dup ENSP00000376584.1:n.*99_*102dup
ENST00000442944.6:c.*99_*102dup ENSP00000392041.2:n.*99_*102dup
ENST00000537841.5:c.*99_*102dup ENSP00000444730.1:n.*99_*102dup
ENST00000539045.1:n.684_687dup
ENST00000542729.5:c.*99_*102dup ENSP00000443058.1:n.*99_*102dup
ENST00000543090.5:c.*99_*102dup ENSP00000445429.1:n.*99_*102dup
ENST00000543543.5:n.1660_1663dup
ENST00000544387.5:c.*99_*102dup ENSP00000438424.1:n.*99_*102dup
ENST00000546226.5:n.1947_1950dup
NM_000190.3:c.*99_*102dup NP_000181.2:n.*99_*102dup
NM_001024382.1:c.*99_*102dup NP_001019553.1:n.*99_*102dup
NM_001258208.1:c.*99_*102dup NP_001245137.1:n.*99_*102dup
NM_001258209.1:c.*99_*102dup NP_001245138.1:n.*99_*102dup
XM_005271531.1:c.*99_*102dup XP_005271588.1:n.*99_*102dup
XM_005271532.1:c.*99_*102dup XP_005271589.1:n.*99_*102dup
XM_005271533.2:c.*99_*102dup XP_005271590.1:n.*99_*102dup
XM_011542796.1:c.*99_*102dup XP_011541098.1:n.*99_*102dup
NM_000190.4:c.*99_*102dup MANE Select NP_000181.2:n.*99_*102dup
NM_001024382.2:c.*99_*102dup NP_001019553.1:n.*99_*102dup
XM_005271533.3:c.*99_*102dup XP_005271590.1:n.*99_*102dup
XM_017017629.1:c.*99_*102dup XP_016873118.1:n.*99_*102dup
XM_024448460.1:c.*99_*102dup XP_024304228.1:n.*99_*102dup
NM_001258208.2:c.*99_*102dup NP_001245137.1:n.*99_*102dup
NM_001258209.2:c.*99_*102dup NP_001245138.1:n.*99_*102dup