Canonical Allele Identifier: CA2793833133

Gene: HMBS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092546_119092547insTTGGGTGTGTTT , CM000673.2:g.119092546_119092547insTTGGGTGTGTTT	GRCh38
NC_000011.9:g.118963256_118963257insTTGGGTGTGTTT , CM000673.1:g.118963256_118963257insTTGGGTGTGTTT	GRCh37
NC_000011.8:g.118468466_118468467insTTGGGTGTGTTT	NCBI36
NG_008093.1:g.12670_12671insTTGGGTGTGTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.606+23_606+24insTTGGGTGTGTTT	ENSP00000509288.1:n.606+23_606+24insTTGGGTGTGTTT
ENST00000691144.1:n.2775_2776insTTGGGTGTGTTT
ENST00000691249.1:n.1595+23_1595+24insTTGGGTGTGTTT
ENST00000442944.7:c.753+23_753+24insTTGGGTGTGTTT	ENSP00000392041.3:n.753+23_753+24insTTGGGTGTGTTT
ENST00000640813.1:c.*8+23_*8+24insTTGGGTGTGTTT	ENSP00000491061.1:n.*8+23_*8+24insTTGGGTGTGTTT
ENST00000648026.1:c.665+23_665+24insTTGGGTGTGTTT	ENSP00000498044.1:n.665+23_665+24insTTGGGTGTGTTT
ENST00000648374.1:c.720+23_720+24insTTGGGTGTGTTT	ENSP00000497255.1:n.720+23_720+24insTTGGGTGTGTTT
ENST00000649823.1:n.1228+23_1228+24insTTGGGTGTGTTT
ENST00000650101.1:c.702+23_702+24insTTGGGTGTGTTT	ENSP00000496970.1:n.702+23_702+24insTTGGGTGTGTTT
ENST00000650307.1:n.1597+23_1597+24insTTGGGTGTGTTT
ENST00000652429.1:c.771+23_771+24insTTGGGTGTGTTT MANE Select	ENSP00000498786.1:n.771+23_771+24insTTGGGTGTGTTT
ENST00000278715.7:c.771+23_771+24insTTGGGTGTGTTT	ENSP00000278715.3:n.771+23_771+24insTTGGGTGTGTTT
ENST00000392841.1:c.720+23_720+24insTTGGGTGTGTTT	ENSP00000376584.1:n.720+23_720+24insTTGGGTGTGTTT
ENST00000442944.6:c.720+23_720+24insTTGGGTGTGTTT	ENSP00000392041.2:n.720+23_720+24insTTGGGTGTGTTT
ENST00000537841.5:c.720+23_720+24insTTGGGTGTGTTT	ENSP00000444730.1:n.720+23_720+24insTTGGGTGTGTTT
ENST00000542044.5:n.1216+23_1216+24insTTGGGTGTGTTT
ENST00000542729.5:c.601-212_601-211insTTGGGTGTGTTT	ENSP00000443058.1:n.601-212_601-211insTTGGGTGTGTTT
ENST00000543090.5:c.678+23_678+24insTTGGGTGTGTTT	ENSP00000445429.1:n.678+23_678+24insTTGGGTGTGTTT
ENST00000543543.5:n.1246+23_1246+24insTTGGGTGTGTTT
ENST00000544182.1:n.1009_1010insTTGGGTGTGTTT
ENST00000544387.5:c.652-212_652-211insTTGGGTGTGTTT	ENSP00000438424.1:n.652-212_652-211insTTGGGTGTGTTT
ENST00000546226.5:n.1322_1323insTTGGGTGTGTTT
NM_000190.3:c.771+23_771+24insTTGGGTGTGTTT	NP_000181.2:n.771+23_771+24insTTGGGTGTGTTT
NM_001024382.1:c.720+23_720+24insTTGGGTGTGTTT	NP_001019553.1:n.720+23_720+24insTTGGGTGTGTTT
NM_001258208.1:c.652-212_652-211insTTGGGTGTGTTT	NP_001245137.1:n.652-212_652-211insTTGGGTGTGTTT
NM_001258209.1:c.601-212_601-211insTTGGGTGTGTTT	NP_001245138.1:n.601-212_601-211insTTGGGTGTGTTT
XM_005271531.1:c.720+23_720+24insTTGGGTGTGTTT	XP_005271588.1:n.720+23_720+24insTTGGGTGTGTTT
XM_005271532.1:c.720+23_720+24insTTGGGTGTGTTT	XP_005271589.1:n.720+23_720+24insTTGGGTGTGTTT
XM_005271533.2:c.717+23_717+24insTTGGGTGTGTTT	XP_005271590.1:n.717+23_717+24insTTGGGTGTGTTT
XM_011542796.1:c.606+23_606+24insTTGGGTGTGTTT	XP_011541098.1:n.606+23_606+24insTTGGGTGTGTTT
NM_000190.4:c.771+23_771+24insTTGGGTGTGTTT MANE Select	NP_000181.2:n.771+23_771+24insTTGGGTGTGTTT
NM_001024382.2:c.720+23_720+24insTTGGGTGTGTTT	NP_001019553.1:n.720+23_720+24insTTGGGTGTGTTT
XM_005271533.3:c.717+23_717+24insTTGGGTGTGTTT	XP_005271590.1:n.717+23_717+24insTTGGGTGTGTTT
XM_017017629.1:c.720+23_720+24insTTGGGTGTGTTT	XP_016873118.1:n.720+23_720+24insTTGGGTGTGTTT
XM_024448460.1:c.598-212_598-211insTTGGGTGTGTTT	XP_024304228.1:n.598-212_598-211insTTGGGTGTGTTT
NM_001258208.2:c.652-212_652-211insTTGGGTGTGTTT	NP_001245137.1:n.652-212_652-211insTTGGGTGTGTTT
NM_001258209.2:c.601-212_601-211insTTGGGTGTGTTT	NP_001245138.1:n.601-212_601-211insTTGGGTGTGTTT