Canonical Allele Identifier: CA477123544

Gene: HMBS

Linked Data

• gnomAD v4: 11-119088640-T-C
• MyVariant Identifiers: chr11:g.118959350T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119088640T>C , CM000673.2:g.119088640T>C	GRCh38
NC_000011.9:g.118959350T>C , CM000673.1:g.118959350T>C	GRCh37
NC_000011.8:g.118464560T>C	NCBI36
NG_008093.1:g.8764T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.-73T>C	ENSP00000509288.1:n.-73T>C
ENST00000686690.1:n.255T>C
ENST00000691144.1:n.1375T>C
ENST00000691249.1:n.677T>C
ENST00000442944.7:c.93T>C	ENSP00000392041.3:p.Ala31=
ENST00000534956.2:n.42T>C
ENST00000536813.6:c.42T>C	ENSP00000438726.2:p.Ala14=
ENST00000546302.6:c.93T>C	ENSP00000445599.1:p.Ala31=
ENST00000640813.1:c.42T>C	ENSP00000491061.1:p.Ala14=
ENST00000648026.1:c.87T>C	ENSP00000498044.1:p.Ala29=
ENST00000648374.1:c.42T>C	ENSP00000497255.1:p.Ala14=
ENST00000648488.1:c.42T>C	ENSP00000498079.1:p.Ala14=
ENST00000649823.1:n.310T>C
ENST00000649868.1:c.34-460T>C	ENSP00000497548.1:n.34-460T>C
ENST00000650101.1:c.42T>C	ENSP00000496970.1:p.Ala14=
ENST00000650307.1:n.545T>C
ENST00000652429.1:c.93T>C MANE Select	ENSP00000498786.1:p.Ala31=
ENST00000278715.7:c.93T>C	ENSP00000278715.3:p.Ala31=
ENST00000392841.1:c.42T>C	ENSP00000376584.1:p.Ala14=
ENST00000442944.6:c.42T>C	ENSP00000392041.2:p.Ala14=
ENST00000534956.1:n.9T>C
ENST00000535253.5:c.42T>C	ENSP00000442079.1:p.Ala14=
ENST00000535793.5:c.39T>C	ENSP00000439904.1:p.Ala13=
ENST00000536185.5:n.261T>C
ENST00000536813.5:c.93T>C	ENSP00000438726.1:p.Ala31=
ENST00000537841.5:c.42T>C	ENSP00000444730.1:p.Ala14=
ENST00000539986.5:c.42T>C	ENSP00000440092.1:p.Ala14=
ENST00000542044.5:n.164T>C
ENST00000542345.5:n.231T>C
ENST00000542729.5:c.42T>C	ENSP00000443058.1:p.Ala14=
ENST00000542822.5:c.184T>C	ENSP00000444817.1:p.Ser62Pro
ENST00000543090.5:c.39T>C	ENSP00000445429.1:p.Ala13=
ENST00000543543.5:n.328T>C
ENST00000543821.5:n.239T>C
ENST00000544360.5:n.61T>C
ENST00000544387.5:c.93T>C	ENSP00000438424.1:p.Ala31=
ENST00000545621.5:c.93T>C	ENSP00000444849.1:p.Ala31=
ENST00000545901.5:n.246T>C
ENST00000546226.5:n.152T>C
ENST00000546302.5:c.93T>C	ENSP00000445599.1:p.Ala31=
NM_000190.3:c.93T>C	NP_000181.2:p.Ala31=
NM_001024382.1:c.42T>C	NP_001019553.1:p.Ala14=
NM_001258208.1:c.93T>C	NP_001245137.1:p.Ala31=
NM_001258209.1:c.42T>C	NP_001245138.1:p.Ala14=
XM_005271531.1:c.42T>C	XP_005271588.1:p.Ala14=
XM_005271532.1:c.42T>C	XP_005271589.1:p.Ala14=
XM_005271533.2:c.39T>C	XP_005271590.1:p.Ala13=
XM_011542796.1:c.-73T>C	XP_011541098.1:n.-73T>C
NM_000190.4:c.93T>C MANE Select	NP_000181.2:p.Ala31=
NM_001024382.2:c.42T>C	NP_001019553.1:p.Ala14=
XM_005271533.3:c.39T>C	XP_005271590.1:p.Ala13=
XM_017017629.1:c.42T>C	XP_016873118.1:p.Ala14=
XM_024448460.1:c.39T>C	XP_024304228.1:p.Ala13=
NM_001258208.2:c.93T>C	NP_001245137.1:p.Ala31=
NM_001258209.2:c.42T>C	NP_001245138.1:p.Ala14=