Canonical Allele Identifier: CA477123625

Gene: HMBS

Linked Data

• gnomAD v4: 11-119088694-G-A
• MyVariant Identifiers: chr11:g.118959404G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119088694G>A , CM000673.2:g.119088694G>A	GRCh38
NC_000011.9:g.118959404G>A , CM000673.1:g.118959404G>A	GRCh37
NC_000011.8:g.118464614G>A	NCBI36
NG_008093.1:g.8818G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.-19G>A	ENSP00000509288.1:n.-19G>A
ENST00000686690.1:n.309G>A
ENST00000691144.1:n.1429G>A
ENST00000691249.1:n.731G>A
ENST00000442944.7:c.147G>A	ENSP00000392041.3:p.Leu49=
ENST00000534956.2:n.96G>A
ENST00000536813.6:c.96G>A	ENSP00000438726.2:p.Leu32=
ENST00000546302.6:c.147G>A	ENSP00000445599.1:p.Leu49=
ENST00000640813.1:c.96G>A	ENSP00000491061.1:p.Leu32=
ENST00000648026.1:c.141G>A	ENSP00000498044.1:p.Leu47=
ENST00000648374.1:c.96G>A	ENSP00000497255.1:p.Leu32=
ENST00000648488.1:c.96G>A	ENSP00000498079.1:p.Leu32=
ENST00000649823.1:n.364G>A
ENST00000649868.1:c.34-406G>A	ENSP00000497548.1:n.34-406G>A
ENST00000650101.1:c.96G>A	ENSP00000496970.1:p.Leu32=
ENST00000650307.1:n.599G>A
ENST00000652429.1:c.147G>A MANE Select	ENSP00000498786.1:p.Leu49=
ENST00000278715.7:c.147G>A	ENSP00000278715.3:p.Leu49=
ENST00000392841.1:c.96G>A	ENSP00000376584.1:p.Leu32=
ENST00000442944.6:c.96G>A	ENSP00000392041.2:p.Leu32=
ENST00000534956.1:n.63G>A
ENST00000535253.5:c.96G>A	ENSP00000442079.1:p.Leu32=
ENST00000535793.5:c.93G>A	ENSP00000439904.1:p.Leu31=
ENST00000536185.5:n.315G>A
ENST00000536813.5:c.147G>A	ENSP00000438726.1:p.Leu49=
ENST00000537841.5:c.96G>A	ENSP00000444730.1:p.Leu32=
ENST00000539986.5:c.96G>A	ENSP00000440092.1:p.Leu32=
ENST00000542044.5:n.218G>A
ENST00000542345.5:n.285G>A
ENST00000542729.5:c.96G>A	ENSP00000443058.1:p.Leu32=
ENST00000542822.5:c.238G>A	ENSP00000444817.1:p.Ala80Thr
ENST00000543090.5:c.93G>A	ENSP00000445429.1:p.Leu31=
ENST00000543543.5:n.382G>A
ENST00000543821.5:n.293G>A
ENST00000544360.5:n.115G>A
ENST00000544387.5:c.147G>A	ENSP00000438424.1:p.Leu49=
ENST00000545621.5:c.147G>A	ENSP00000444849.1:p.Leu49=
ENST00000545901.5:n.300G>A
ENST00000546226.5:n.206G>A
ENST00000546302.5:c.147G>A	ENSP00000445599.1:p.Leu49=
NM_000190.3:c.147G>A	NP_000181.2:p.Leu49=
NM_001024382.1:c.96G>A	NP_001019553.1:p.Leu32=
NM_001258208.1:c.147G>A	NP_001245137.1:p.Leu49=
NM_001258209.1:c.96G>A	NP_001245138.1:p.Leu32=
XM_005271531.1:c.96G>A	XP_005271588.1:p.Leu32=
XM_005271532.1:c.96G>A	XP_005271589.1:p.Leu32=
XM_005271533.2:c.93G>A	XP_005271590.1:p.Leu31=
XM_011542796.1:c.-19G>A	XP_011541098.1:n.-19G>A
NM_000190.4:c.147G>A MANE Select	NP_000181.2:p.Leu49=
NM_001024382.2:c.96G>A	NP_001019553.1:p.Leu32=
XM_005271533.3:c.93G>A	XP_005271590.1:p.Leu31=
XM_017017629.1:c.96G>A	XP_016873118.1:p.Leu32=
XM_024448460.1:c.93G>A	XP_024304228.1:p.Leu31=
NM_001258208.2:c.147G>A	NP_001245137.1:p.Leu49=
NM_001258209.2:c.96G>A	NP_001245138.1:p.Leu32=