Canonical Allele Identifier: CA382899434

Gene: HMBS

Linked Data

• dbSNP Id: rs1201268870
• gnomAD v4: 11-119093168-C-A
• MyVariant Identifiers: chr11:g.118963878C>A (hg19) ; chr11:g.119093168C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119093168C>A , CM000673.2:g.119093168C>A	GRCh38
NC_000011.9:g.118963878C>A , CM000673.1:g.118963878C>A	GRCh37
NC_000011.8:g.118469088C>A	NCBI36
NG_008093.1:g.13292C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000686218.1:c.806C>A	ENSP00000509288.1:p.Pro269Gln
ENST00000691144.1:n.3186C>A
ENST00000691249.1:n.1795C>A
ENST00000442944.7:c.953C>A	ENSP00000392041.3:p.Pro318Gln
ENST00000640813.1:c.*208C>A	ENSP00000491061.1:n.*208C>A
ENST00000648026.1:c.865C>A	ENSP00000498044.1:n.865C>A
ENST00000648374.1:c.920C>A	ENSP00000497255.1:p.Pro307Gln
ENST00000650101.1:c.902C>A	ENSP00000496970.1:p.Pro301Gln
ENST00000650307.1:n.1797C>A
ENST00000652429.1:c.971C>A MANE Select	ENSP00000498786.1:p.Pro324Gln
ENST00000278715.7:c.971C>A	ENSP00000278715.3:p.Pro324Gln
ENST00000392841.1:c.920C>A	ENSP00000376584.1:p.Pro307Gln
ENST00000442944.6:c.920C>A	ENSP00000392041.2:p.Pro307Gln
ENST00000537841.5:c.920C>A	ENSP00000444730.1:p.Pro307Gln
ENST00000539045.1:n.470C>A
ENST00000542044.5:n.1416C>A
ENST00000542729.5:c.800C>A	ENSP00000443058.1:p.Pro267Gln
ENST00000543090.5:c.878C>A	ENSP00000445429.1:p.Pro293Gln
ENST00000543543.5:n.1446C>A
ENST00000544182.1:n.1420C>A
ENST00000544387.5:c.851C>A	ENSP00000438424.1:p.Pro284Gln
ENST00000546226.5:n.1733C>A
NM_000190.3:c.971C>A	NP_000181.2:p.Pro324Gln
NM_001024382.1:c.920C>A	NP_001019553.1:p.Pro307Gln
NM_001258208.1:c.851C>A	NP_001245137.1:p.Pro284Gln
NM_001258209.1:c.800C>A	NP_001245138.1:p.Pro267Gln
XM_005271531.1:c.920C>A	XP_005271588.1:p.Pro307Gln
XM_005271532.1:c.920C>A	XP_005271589.1:p.Pro307Gln
XM_005271533.2:c.917C>A	XP_005271590.1:p.Pro306Gln
XM_011542796.1:c.806C>A	XP_011541098.1:p.Pro269Gln
NM_000190.4:c.971C>A MANE Select	NP_000181.2:p.Pro324Gln
NM_001024382.2:c.920C>A	NP_001019553.1:p.Pro307Gln
XM_005271533.3:c.917C>A	XP_005271590.1:p.Pro306Gln
XM_017017629.1:c.920C>A	XP_016873118.1:p.Pro307Gln
XM_024448460.1:c.797C>A	XP_024304228.1:p.Pro266Gln
NM_001258208.2:c.851C>A	NP_001245137.1:p.Pro284Gln
NM_001258209.2:c.800C>A	NP_001245138.1:p.Pro267Gln