Canonical Allele Identifier: CA477126456

Gene: HMBS

Linked Data

• dbSNP Id: rs111268492
• gnomAD v2: 11-118962696-C-CA
• gnomAD v3: 11-119091986-C-CA
• gnomAD v4: 11-119091986-C-CA
• MyVariant Identifiers: chr11:g.118962698_118962699insA (hg19) ; chr11:g.118962696_118962697insA (hg19) ; chr11:g.119091988_119091989insA (hg38) ; chr11:g.119091986_119091987insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092001dup , CM000673.2:g.119092001dup	GRCh38
NC_000011.9:g.118962711dup , CM000673.1:g.118962711dup	GRCh37
NC_000011.8:g.118467921dup	NCBI36
NG_008093.1:g.12125dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.448-124dup	ENSP00000509288.1:n.448-124dup
ENST00000691144.1:n.2354-124dup
ENST00000691249.1:n.1197-124dup
ENST00000442944.7:c.595-124dup	ENSP00000392041.3:n.595-124dup
ENST00000536813.6:c.562-124dup	ENSP00000438726.2:n.562-124dup
ENST00000546302.6:c.535-124dup	ENSP00000445599.1:n.535-124dup
ENST00000640813.1:c.461+127dup	ENSP00000491061.1:n.461+127dup
ENST00000648026.1:c.507-124dup	ENSP00000498044.1:n.507-124dup
ENST00000648374.1:c.562-124dup	ENSP00000497255.1:n.562-124dup
ENST00000648488.1:c.*86-124dup	ENSP00000498079.1:n.*86-124dup
ENST00000649823.1:n.830-124dup
ENST00000650101.1:c.544-124dup	ENSP00000496970.1:n.544-124dup
ENST00000650307.1:n.1439-124dup
ENST00000652429.1:c.613-124dup MANE Select	ENSP00000498786.1:n.613-124dup
ENST00000278715.7:c.613-124dup	ENSP00000278715.3:n.613-124dup
ENST00000392841.1:c.562-124dup	ENSP00000376584.1:n.562-124dup
ENST00000442944.6:c.562-124dup	ENSP00000392041.2:n.562-124dup
ENST00000537841.5:c.562-124dup	ENSP00000444730.1:n.562-124dup
ENST00000542044.5:n.1058-124dup
ENST00000542345.5:n.751-124dup
ENST00000542729.5:c.562-124dup	ENSP00000443058.1:n.562-124dup
ENST00000543090.5:c.559-403dup	ENSP00000445429.1:n.559-403dup
ENST00000543543.5:n.848-124dup
ENST00000544182.1:n.464dup
ENST00000544387.5:c.613-124dup	ENSP00000438424.1:n.613-124dup
ENST00000545621.5:c.*508-124dup	ENSP00000444849.1:n.*508-124dup
ENST00000546226.5:n.901-124dup
ENST00000546302.5:c.535-124dup	ENSP00000445599.1:n.535-124dup
NM_000190.3:c.613-124dup	NP_000181.2:n.613-124dup
NM_001024382.1:c.562-124dup	NP_001019553.1:n.562-124dup
NM_001258208.1:c.613-124dup	NP_001245137.1:n.613-124dup
NM_001258209.1:c.562-124dup	NP_001245138.1:n.562-124dup
XM_005271531.1:c.562-124dup	XP_005271588.1:n.562-124dup
XM_005271532.1:c.562-124dup	XP_005271589.1:n.562-124dup
XM_005271533.2:c.559-124dup	XP_005271590.1:n.559-124dup
XM_011542796.1:c.448-124dup	XP_011541098.1:n.448-124dup
NM_000190.4:c.613-124dup MANE Select	NP_000181.2:n.613-124dup
NM_001024382.2:c.562-124dup	NP_001019553.1:n.562-124dup
XM_005271533.3:c.559-124dup	XP_005271590.1:n.559-124dup
XM_017017629.1:c.562-124dup	XP_016873118.1:n.562-124dup
XM_024448460.1:c.559-124dup	XP_024304228.1:n.559-124dup
NM_001258208.2:c.613-124dup	NP_001245137.1:n.613-124dup
NM_001258209.2:c.562-124dup	NP_001245138.1:n.562-124dup