Canonical Allele Identifier: CA382897120
Gene: HMBS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119092412G>C , CM000673.2:g.119092412G>C GRCh38
NC_000011.9:g.118963122G>C , CM000673.1:g.118963122G>C GRCh37
NC_000011.8:g.118468332G>C NCBI36
NG_008093.1:g.12536G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000686218.1:c.495G>C ENSP00000509288.1:p.Leu165Phe
ENST00000691144.1:n.2641G>C
ENST00000691249.1:n.1484G>C
ENST00000442944.7:c.642G>C ENSP00000392041.3:p.Leu214Phe
ENST00000536813.6:c.609G>C ENSP00000438726.2:p.Leu203Phe
ENST00000640813.1:c.470G>C ENSP00000491061.1:p.Trp157Ser
ENST00000648026.1:c.554G>C ENSP00000498044.1:p.Trp185Ser
ENST00000648374.1:c.609G>C ENSP00000497255.1:p.Leu203Phe
ENST00000649823.1:n.1117G>C
ENST00000650101.1:c.591G>C ENSP00000496970.1:p.Leu197Phe
ENST00000650307.1:n.1486G>C
ENST00000652429.1:c.660G>C MANE Select ENSP00000498786.1:p.Leu220Phe
ENST00000278715.7:c.660G>C ENSP00000278715.3:p.Leu220Phe
ENST00000392841.1:c.609G>C ENSP00000376584.1:p.Leu203Phe
ENST00000442944.6:c.609G>C ENSP00000392041.2:p.Leu203Phe
ENST00000537841.5:c.609G>C ENSP00000444730.1:p.Leu203Phe
ENST00000542044.5:n.1105G>C
ENST00000542729.5:c.600+249G>C ENSP00000443058.1:n.600+249G>C
ENST00000543090.5:c.567G>C ENSP00000445429.1:p.Leu189Phe
ENST00000543543.5:n.1135G>C
ENST00000544182.1:n.875G>C
ENST00000544387.5:c.651+249G>C ENSP00000438424.1:n.651+249G>C
ENST00000545621.5:c.*795G>C ENSP00000444849.1:n.*795G>C
ENST00000546226.5:n.1188G>C
NM_000190.3:c.660G>C NP_000181.2:p.Leu220Phe
NM_001024382.1:c.609G>C NP_001019553.1:p.Leu203Phe
NM_001258208.1:c.651+249G>C NP_001245137.1:n.651+249G>C
NM_001258209.1:c.600+249G>C NP_001245138.1:n.600+249G>C
XM_005271531.1:c.609G>C XP_005271588.1:p.Leu203Phe
XM_005271532.1:c.609G>C XP_005271589.1:p.Leu203Phe
XM_005271533.2:c.606G>C XP_005271590.1:p.Leu202Phe
XM_011542796.1:c.495G>C XP_011541098.1:p.Leu165Phe
NM_000190.4:c.660G>C MANE Select NP_000181.2:p.Leu220Phe
NM_001024382.2:c.609G>C NP_001019553.1:p.Leu203Phe
XM_005271533.3:c.606G>C XP_005271590.1:p.Leu202Phe
XM_017017629.1:c.609G>C XP_016873118.1:p.Leu203Phe
XM_024448460.1:c.597+249G>C XP_024304228.1:n.597+249G>C
NM_001258208.2:c.651+249G>C NP_001245137.1:n.651+249G>C
NM_001258209.2:c.600+249G>C NP_001245138.1:n.600+249G>C