Canonical Allele Identifier: CA6314196

Gene: HMBS

Linked Data

• ClinVar Variation Id: 1554998
• ClinVar RCV Id: RCV002192647
• dbSNP Id: rs760626480
• ExAC: 11:118963451 AG / A
• gnomAD v2: 11-118963451-AG-A
• gnomAD v3: 11-119092741-AG-A
• gnomAD v4: 11-119092741-AG-A
• MyVariant Identifiers: chr11:g.118963452del (hg19) ; chr11:g.119092742del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092742del , CM000673.2:g.119092742del	GRCh38
NC_000011.9:g.118963452del , CM000673.1:g.118963452del	GRCh37
NC_000011.8:g.118468662del	NCBI36
NG_008093.1:g.12866del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.607-16del	ENSP00000509288.1:n.607-16del
ENST00000691144.1:n.2971del
ENST00000691249.1:n.1596-16del
ENST00000442944.7:c.754-16del	ENSP00000392041.3:n.754-16del
ENST00000640813.1:c.*9-16del	ENSP00000491061.1:n.*9-16del
ENST00000648026.1:c.666-16del	ENSP00000498044.1:n.666-16del
ENST00000648374.1:c.721-16del	ENSP00000497255.1:n.721-16del
ENST00000649823.1:n.1229-16del
ENST00000650101.1:c.703-16del	ENSP00000496970.1:n.703-16del
ENST00000650307.1:n.1598-16del
ENST00000652429.1:c.772-16del MANE Select	ENSP00000498786.1:n.772-16del
ENST00000278715.7:c.772-16del	ENSP00000278715.3:n.772-16del
ENST00000392841.1:c.721-16del	ENSP00000376584.1:n.721-16del
ENST00000442944.6:c.721-16del	ENSP00000392041.2:n.721-16del
ENST00000537841.5:c.721-16del	ENSP00000444730.1:n.721-16del
ENST00000539045.1:n.132del
ENST00000542044.5:n.1217-16del
ENST00000542729.5:c.601-16del	ENSP00000443058.1:n.601-16del
ENST00000543090.5:c.679-16del	ENSP00000445429.1:n.679-16del
ENST00000543543.5:n.1247-16del
ENST00000544182.1:n.1205del
ENST00000544387.5:c.652-16del	ENSP00000438424.1:n.652-16del
ENST00000546226.5:n.1518del
NM_000190.3:c.772-16del	NP_000181.2:n.772-16del
NM_001024382.1:c.721-16del	NP_001019553.1:n.721-16del
NM_001258208.1:c.652-16del	NP_001245137.1:n.652-16del
NM_001258209.1:c.601-16del	NP_001245138.1:n.601-16del
XM_005271531.1:c.721-16del	XP_005271588.1:n.721-16del
XM_005271532.1:c.721-16del	XP_005271589.1:n.721-16del
XM_005271533.2:c.718-16del	XP_005271590.1:n.718-16del
XM_011542796.1:c.607-16del	XP_011541098.1:n.607-16del
NM_000190.4:c.772-16del MANE Select	NP_000181.2:n.772-16del
NM_001024382.2:c.721-16del	NP_001019553.1:n.721-16del
XM_005271533.3:c.718-16del	XP_005271590.1:n.718-16del
XM_017017629.1:c.721-16del	XP_016873118.1:n.721-16del
XM_024448460.1:c.598-16del	XP_024304228.1:n.598-16del
NM_001258208.2:c.652-16del	NP_001245137.1:n.652-16del
NM_001258209.2:c.601-16del	NP_001245138.1:n.601-16del