Canonical Allele Identifier: CA382896686

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118962845C>G (hg19) ; chr11:g.119092135C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092135C>G , CM000673.2:g.119092135C>G	GRCh38
NC_000011.9:g.118962845C>G , CM000673.1:g.118962845C>G	GRCh37
NC_000011.8:g.118468055C>G	NCBI36
NG_008093.1:g.12259C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.458C>G	ENSP00000509288.1:p.Pro153Arg
ENST00000691144.1:n.2364C>G
ENST00000691249.1:n.1207C>G
ENST00000442944.7:c.605C>G	ENSP00000392041.3:p.Pro202Arg
ENST00000536813.6:c.572C>G	ENSP00000438726.2:p.Pro191Arg
ENST00000546302.6:c.545C>G	ENSP00000445599.1:p.Pro182Arg
ENST00000640813.1:c.461+261C>G	ENSP00000491061.1:n.461+261C>G
ENST00000648026.1:c.517C>G	ENSP00000498044.1:p.Leu173Val
ENST00000648374.1:c.572C>G	ENSP00000497255.1:p.Pro191Arg
ENST00000648488.1:c.*96C>G	ENSP00000498079.1:n.*96C>G
ENST00000649823.1:n.840C>G
ENST00000650101.1:c.554C>G	ENSP00000496970.1:p.Pro185Arg
ENST00000650307.1:n.1449C>G
ENST00000652429.1:c.623C>G MANE Select	ENSP00000498786.1:p.Pro208Arg
ENST00000278715.7:c.623C>G	ENSP00000278715.3:p.Pro208Arg
ENST00000392841.1:c.572C>G	ENSP00000376584.1:p.Pro191Arg
ENST00000442944.6:c.572C>G	ENSP00000392041.2:p.Pro191Arg
ENST00000537841.5:c.572C>G	ENSP00000444730.1:p.Pro191Arg
ENST00000542044.5:n.1068C>G
ENST00000542345.5:n.761C>G
ENST00000542729.5:c.572C>G	ENSP00000443058.1:p.Pro191Arg
ENST00000543090.5:c.559-269C>G	ENSP00000445429.1:n.559-269C>G
ENST00000543543.5:n.858C>G
ENST00000544182.1:n.598C>G
ENST00000544387.5:c.623C>G	ENSP00000438424.1:p.Pro208Arg
ENST00000545621.5:c.*518C>G	ENSP00000444849.1:n.*518C>G
ENST00000546226.5:n.911C>G
ENST00000546302.5:c.545C>G	ENSP00000445599.1:p.Pro182Arg
NM_000190.3:c.623C>G	NP_000181.2:p.Pro208Arg
NM_001024382.1:c.572C>G	NP_001019553.1:p.Pro191Arg
NM_001258208.1:c.623C>G	NP_001245137.1:p.Pro208Arg
NM_001258209.1:c.572C>G	NP_001245138.1:p.Pro191Arg
XM_005271531.1:c.572C>G	XP_005271588.1:p.Pro191Arg
XM_005271532.1:c.572C>G	XP_005271589.1:p.Pro191Arg
XM_005271533.2:c.569C>G	XP_005271590.1:p.Pro190Arg
XM_011542796.1:c.458C>G	XP_011541098.1:p.Pro153Arg
NM_000190.4:c.623C>G MANE Select	NP_000181.2:p.Pro208Arg
NM_001024382.2:c.572C>G	NP_001019553.1:p.Pro191Arg
XM_005271533.3:c.569C>G	XP_005271590.1:p.Pro190Arg
XM_017017629.1:c.572C>G	XP_016873118.1:p.Pro191Arg
XM_024448460.1:c.569C>G	XP_024304228.1:p.Pro190Arg
NM_001258208.2:c.623C>G	NP_001245137.1:p.Pro208Arg
NM_001258209.2:c.572C>G	NP_001245138.1:p.Pro191Arg