Canonical Allele Identifier: CA2616354832

Gene: HMBS

Linked Data

• gnomAD v4: 11-119092317-GGAGCAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092319_119092324del , CM000673.2:g.119092319_119092324del	GRCh38
NC_000011.9:g.118963029_118963034del , CM000673.1:g.118963029_118963034del	GRCh37
NC_000011.8:g.118468239_118468244del	NCBI36
NG_008093.1:g.12443_12448del

Transcript Alleles

HGVS	Amino-acid change
ENST00000686218.1:c.487-85_487-80del	ENSP00000509288.1:n.487-85_487-80del
ENST00000691144.1:n.2548_2553del
ENST00000691249.1:n.1391_1396del
ENST00000442944.7:c.634-85_634-80del	ENSP00000392041.3:n.634-85_634-80del
ENST00000536813.6:c.601-85_601-80del	ENSP00000438726.2:n.601-85_601-80del
ENST00000640813.1:c.462-85_462-80del	ENSP00000491061.1:n.462-85_462-80del
ENST00000648026.1:c.546-85_546-80del	ENSP00000498044.1:n.546-85_546-80del
ENST00000648374.1:c.601-85_601-80del	ENSP00000497255.1:n.601-85_601-80del
ENST00000649823.1:n.1024_1029del
ENST00000650101.1:c.583-85_583-80del	ENSP00000496970.1:n.583-85_583-80del
ENST00000650307.1:n.1478-85_1478-80del
ENST00000652429.1:c.652-85_652-80del MANE Select	ENSP00000498786.1:n.652-85_652-80del
ENST00000278715.7:c.652-85_652-80del	ENSP00000278715.3:n.652-85_652-80del
ENST00000392841.1:c.601-85_601-80del	ENSP00000376584.1:n.601-85_601-80del
ENST00000442944.6:c.601-85_601-80del	ENSP00000392041.2:n.601-85_601-80del
ENST00000537841.5:c.601-85_601-80del	ENSP00000444730.1:n.601-85_601-80del
ENST00000542044.5:n.1097-85_1097-80del
ENST00000542729.5:c.600+156_600+161del	ENSP00000443058.1:n.600+156_600+161del
ENST00000543090.5:c.559-85_559-80del	ENSP00000445429.1:n.559-85_559-80del
ENST00000543543.5:n.1042_1047del
ENST00000544182.1:n.782_787del
ENST00000544387.5:c.651+156_651+161del	ENSP00000438424.1:n.651+156_651+161del
ENST00000545621.5:c.*702_*707del	ENSP00000444849.1:n.*702_*707del
ENST00000546226.5:n.1095_1100del
NM_000190.3:c.652-85_652-80del	NP_000181.2:n.652-85_652-80del
NM_001024382.1:c.601-85_601-80del	NP_001019553.1:n.601-85_601-80del
NM_001258208.1:c.651+156_651+161del	NP_001245137.1:n.651+156_651+161del
NM_001258209.1:c.600+156_600+161del	NP_001245138.1:n.600+156_600+161del
XM_005271531.1:c.601-85_601-80del	XP_005271588.1:n.601-85_601-80del
XM_005271532.1:c.601-85_601-80del	XP_005271589.1:n.601-85_601-80del
XM_005271533.2:c.598-85_598-80del	XP_005271590.1:n.598-85_598-80del
XM_011542796.1:c.487-85_487-80del	XP_011541098.1:n.487-85_487-80del
NM_000190.4:c.652-85_652-80del MANE Select	NP_000181.2:n.652-85_652-80del
NM_001024382.2:c.601-85_601-80del	NP_001019553.1:n.601-85_601-80del
XM_005271533.3:c.598-85_598-80del	XP_005271590.1:n.598-85_598-80del
XM_017017629.1:c.601-85_601-80del	XP_016873118.1:n.601-85_601-80del
XM_024448460.1:c.597+156_597+161del	XP_024304228.1:n.597+156_597+161del
NM_001258208.2:c.651+156_651+161del	NP_001245137.1:n.651+156_651+161del
NM_001258209.2:c.600+156_600+161del	NP_001245138.1:n.600+156_600+161del