Canonical Allele Identifier: CA2695215719

Gene: HMBS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119089102del , CM000673.2:g.119089102del	GRCh38
NC_000011.9:g.118959812del , CM000673.1:g.118959812del	GRCh37
NC_000011.8:g.118465022del	NCBI36
NG_008093.1:g.9226del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.16del	ENSP00000509288.1:p.Asp6ThrfsTer?
ENST00000686690.1:n.717del
ENST00000691144.1:n.1837del
ENST00000691249.1:n.765del
ENST00000442944.7:c.163del
ENST00000534956.2:n.130del
ENST00000536813.6:c.130del	ENSP00000438726.2:p.Asp44ThrfsTer?
ENST00000546302.6:c.181del	ENSP00000445599.1:p.Asp61ThrfsTer?
ENST00000640813.1:c.130del	ENSP00000491061.1:p.Asp44ThrfsTer?
ENST00000648026.1:c.175del	ENSP00000498044.1:p.Asp59ThrfsTer?
ENST00000648374.1:c.130del	ENSP00000497255.1:p.Asp44ThrfsTer?
ENST00000648488.1:c.130del	ENSP00000498079.1:p.Asp44ThrfsTer?
ENST00000649823.1:n.398del
ENST00000649868.1:c.36del
ENST00000650101.1:c.112del
ENST00000650307.1:n.1007del
ENST00000652429.1:c.181del MANE Select	ENSP00000498786.1:p.Asp61ThrfsTer?
ENST00000278715.7:c.181del	ENSP00000278715.3:p.Asp61ThrfsTer?
ENST00000392841.1:c.130del	ENSP00000376584.1:p.Asp44ThrfsTer?
ENST00000442944.6:c.130del	ENSP00000392041.2:p.Asp44ThrfsTer?
ENST00000534956.1:n.97del
ENST00000535253.5:c.130del	ENSP00000442079.1:p.Asp44ThrfsTer?
ENST00000535793.5:c.*76del	ENSP00000439904.1:n.*76del
ENST00000536185.5:n.329-115del
ENST00000536813.5:c.163del
ENST00000537841.5:c.130del	ENSP00000444730.1:p.Asp44ThrfsTer?
ENST00000539986.5:c.130del	ENSP00000440092.1:p.Asp44ThrfsTer?
ENST00000542044.5:n.626del
ENST00000542345.5:n.319del
ENST00000542729.5:c.130del	ENSP00000443058.1:p.Asp44ThrfsTer?
ENST00000542822.5:c.*147-115del	ENSP00000444817.1:n.*147-115del
ENST00000543090.5:c.127del	ENSP00000445429.1:p.Asp43ThrfsTer?
ENST00000543543.5:n.416del
ENST00000543821.5:n.327del
ENST00000544360.5:n.149del
ENST00000544387.5:c.181del	ENSP00000438424.1:p.Asp61ThrfsTer?
ENST00000545621.5:c.*76del	ENSP00000444849.1:n.*76del
ENST00000546226.5:n.240del
ENST00000546302.5:c.181del	ENSP00000445599.1:p.Asp61ThrfsTer?
NM_000190.3:c.181del	NP_000181.2:p.Asp61ThrfsTer?
NM_001024382.1:c.130del	NP_001019553.1:p.Asp44ThrfsTer?
NM_001258208.1:c.181del	NP_001245137.1:p.Asp61ThrfsTer?
NM_001258209.1:c.130del	NP_001245138.1:p.Asp44ThrfsTer?
XM_005271531.1:c.130del	XP_005271588.1:p.Asp44ThrfsTer?
XM_005271532.1:c.130del	XP_005271589.1:p.Asp44ThrfsTer?
XM_005271533.2:c.127del	XP_005271590.1:p.Asp43ThrfsTer?
XM_011542796.1:c.16del	XP_011541098.1:p.Asp6ThrfsTer?
NM_000190.4:c.181del MANE Select	NP_000181.2:p.Asp61ThrfsTer?
NM_001024382.2:c.130del	NP_001019553.1:p.Asp44ThrfsTer?
XM_005271533.3:c.127del	XP_005271590.1:p.Asp43ThrfsTer?
XM_017017629.1:c.130del	XP_016873118.1:p.Asp44ThrfsTer?
XM_024448460.1:c.127del	XP_024304228.1:p.Asp43ThrfsTer?
NM_001258208.2:c.181del	NP_001245137.1:p.Asp61ThrfsTer?
NM_001258209.2:c.130del	NP_001245138.1:p.Asp44ThrfsTer?