Canonical Allele Identifier: CA2695215821

Gene: HMBS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092399_119092400delinsTC , CM000673.2:g.119092399_119092400delinsTC	GRCh38
NC_000011.9:g.118963109_118963110delinsTC , CM000673.1:g.118963109_118963110delinsTC	GRCh37
NC_000011.8:g.118468319_118468320delinsTC	NCBI36
NG_008093.1:g.12523_12524delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000686218.1:c.487-5_487-4delinsTC	ENSP00000509288.1:n.487-5_487-4delinsTC
ENST00000691144.1:n.2628_2629delinsTC
ENST00000691249.1:n.1471_1472delinsTC
ENST00000442944.7:c.634-5_634-4delinsTC	ENSP00000392041.3:n.634-5_634-4delinsTC
ENST00000536813.6:c.601-5_601-4delinsTC	ENSP00000438726.2:n.601-5_601-4delinsTC
ENST00000640813.1:c.462-5_462-4delinsTC	ENSP00000491061.1:n.462-5_462-4delinsTC
ENST00000648026.1:c.546-5_546-4delinsTC	ENSP00000498044.1:n.546-5_546-4delinsTC
ENST00000648374.1:c.601-5_601-4delinsTC	ENSP00000497255.1:n.601-5_601-4delinsTC
ENST00000649823.1:n.1104_1105delinsTC
ENST00000650101.1:c.583-5_583-4delinsTC	ENSP00000496970.1:n.583-5_583-4delinsTC
ENST00000650307.1:n.1478-5_1478-4delinsTC
ENST00000652429.1:c.652-5_652-4delinsTC MANE Select	ENSP00000498786.1:n.652-5_652-4delinsTC
ENST00000278715.7:c.652-5_652-4delinsTC	ENSP00000278715.3:n.652-5_652-4delinsTC
ENST00000392841.1:c.601-5_601-4delinsTC	ENSP00000376584.1:n.601-5_601-4delinsTC
ENST00000442944.6:c.601-5_601-4delinsTC	ENSP00000392041.2:n.601-5_601-4delinsTC
ENST00000537841.5:c.601-5_601-4delinsTC	ENSP00000444730.1:n.601-5_601-4delinsTC
ENST00000542044.5:n.1097-5_1097-4delinsTC
ENST00000542729.5:c.600+236_600+237delinsTC	ENSP00000443058.1:n.600+236_600+237delins...
ENST00000543090.5:c.559-5_559-4delinsTC	ENSP00000445429.1:n.559-5_559-4delinsTC
ENST00000543543.5:n.1122_1123delinsTC
ENST00000544182.1:n.862_863delinsTC
ENST00000544387.5:c.651+236_651+237delinsTC	ENSP00000438424.1:n.651+236_651+237delins...
ENST00000545621.5:c.*782_*783delinsTC	ENSP00000444849.1:n.*782_*783delinsTC
ENST00000546226.5:n.1175_1176delinsTC
NM_000190.3:c.652-5_652-4delinsTC	NP_000181.2:n.652-5_652-4delinsTC
NM_001024382.1:c.601-5_601-4delinsTC	NP_001019553.1:n.601-5_601-4delinsTC
NM_001258208.1:c.651+236_651+237delinsTC	NP_001245137.1:n.651+236_651+237delinsTC
NM_001258209.1:c.600+236_600+237delinsTC	NP_001245138.1:n.600+236_600+237delinsTC
XM_005271531.1:c.601-5_601-4delinsTC	XP_005271588.1:n.601-5_601-4delinsTC
XM_005271532.1:c.601-5_601-4delinsTC	XP_005271589.1:n.601-5_601-4delinsTC
XM_005271533.2:c.598-5_598-4delinsTC	XP_005271590.1:n.598-5_598-4delinsTC
XM_011542796.1:c.487-5_487-4delinsTC	XP_011541098.1:n.487-5_487-4delinsTC
NM_000190.4:c.652-5_652-4delinsTC MANE Select	NP_000181.2:n.652-5_652-4delinsTC
NM_001024382.2:c.601-5_601-4delinsTC	NP_001019553.1:n.601-5_601-4delinsTC
XM_005271533.3:c.598-5_598-4delinsTC	XP_005271590.1:n.598-5_598-4delinsTC
XM_017017629.1:c.601-5_601-4delinsTC	XP_016873118.1:n.601-5_601-4delinsTC
XM_024448460.1:c.597+236_597+237delinsTC	XP_024304228.1:n.597+236_597+237delinsTC
NM_001258208.2:c.651+236_651+237delinsTC	NP_001245137.1:n.651+236_651+237delinsTC
NM_001258209.2:c.600+236_600+237delinsTC	NP_001245138.1:n.600+236_600+237delinsTC