Canonical Allele Identifier: CA382899032

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.119093074_119093075del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119093075_119093076del , CM000673.2:g.119093075_119093076del	GRCh38
NC_000011.9:g.118963785_118963786del , CM000673.1:g.118963785_118963786del	GRCh37
NC_000011.8:g.118468995_118468996del	NCBI36
NG_008093.1:g.13199_13200del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.748-35_748-34del	ENSP00000509288.1:n.748-35_748-34del
ENST00000691144.1:n.3128-35_3128-34del
ENST00000691249.1:n.1737-35_1737-34del
ENST00000442944.7:c.895-35_895-34del	ENSP00000392041.3:n.895-35_895-34del
ENST00000640813.1:c.*150-35_*150-34del	ENSP00000491061.1:n.*150-35_*150-34del
ENST00000648026.1:c.807-35_807-34del	ENSP00000498044.1:n.807-35_807-34del
ENST00000648374.1:c.862-35_862-34del	ENSP00000497255.1:n.862-35_862-34del
ENST00000650101.1:c.844-35_844-34del	ENSP00000496970.1:n.844-35_844-34del
ENST00000650307.1:n.1739-35_1739-34del
ENST00000652429.1:c.913-35_913-34del MANE Select	ENSP00000498786.1:n.913-35_913-34del
ENST00000278715.7:c.913-35_913-34del	ENSP00000278715.3:n.913-35_913-34del
ENST00000392841.1:c.862-35_862-34del	ENSP00000376584.1:n.862-35_862-34del
ENST00000442944.6:c.862-35_862-34del	ENSP00000392041.2:n.862-35_862-34del
ENST00000537841.5:c.862-35_862-34del	ENSP00000444730.1:n.862-35_862-34del
ENST00000539045.1:n.412-35_412-34del
ENST00000542044.5:n.1358-35_1358-34del
ENST00000542729.5:c.742-35_742-34del	ENSP00000443058.1:n.742-35_742-34del
ENST00000543090.5:c.820-35_820-34del	ENSP00000445429.1:n.820-35_820-34del
ENST00000543543.5:n.1388-35_1388-34del
ENST00000544182.1:n.1362-35_1362-34del
ENST00000544387.5:c.793-35_793-34del	ENSP00000438424.1:n.793-35_793-34del
ENST00000546226.5:n.1675-35_1675-34del
NM_000190.3:c.913-35_913-34del	NP_000181.2:n.913-35_913-34del
NM_001024382.1:c.862-35_862-34del	NP_001019553.1:n.862-35_862-34del
NM_001258208.1:c.793-35_793-34del	NP_001245137.1:n.793-35_793-34del
NM_001258209.1:c.742-35_742-34del	NP_001245138.1:n.742-35_742-34del
XM_005271531.1:c.862-35_862-34del	XP_005271588.1:n.862-35_862-34del
XM_005271532.1:c.862-35_862-34del	XP_005271589.1:n.862-35_862-34del
XM_005271533.2:c.859-35_859-34del	XP_005271590.1:n.859-35_859-34del
XM_011542796.1:c.748-35_748-34del	XP_011541098.1:n.748-35_748-34del
NM_000190.4:c.913-35_913-34del MANE Select	NP_000181.2:n.913-35_913-34del
NM_001024382.2:c.862-35_862-34del	NP_001019553.1:n.862-35_862-34del
XM_005271533.3:c.859-35_859-34del	XP_005271590.1:n.859-35_859-34del
XM_017017629.1:c.862-35_862-34del	XP_016873118.1:n.862-35_862-34del
XM_024448460.1:c.739-35_739-34del	XP_024304228.1:n.739-35_739-34del
NM_001258208.2:c.793-35_793-34del	NP_001245137.1:n.793-35_793-34del
NM_001258209.2:c.742-35_742-34del	NP_001245138.1:n.742-35_742-34del