Canonical Allele Identifier: CA2575084801

Gene: HMBS

Linked Data

• gnomAD v4: 11-119089777-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119089779del , CM000673.2:g.119089779del	GRCh38
NC_000011.9:g.118960489del , CM000673.1:g.118960489del	GRCh37
NC_000011.8:g.118465699del	NCBI36
NG_008093.1:g.9903del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.179+19del	ENSP00000509288.1:n.179+19del
ENST00000686690.1:n.984del
ENST00000691144.1:n.2085+19del
ENST00000691249.1:n.928+19del
ENST00000442944.7:c.326+19del	ENSP00000392041.3:n.326+19del
ENST00000534956.2:n.293+19del
ENST00000536813.6:c.293+19del	ENSP00000438726.2:n.293+19del
ENST00000546302.6:c.267-211del	ENSP00000445599.1:n.267-211del
ENST00000640813.1:c.293+19del	ENSP00000491061.1:n.293+19del
ENST00000648026.1:c.338+19del	ENSP00000498044.1:n.338+19del
ENST00000648374.1:c.293+19del	ENSP00000497255.1:n.293+19del
ENST00000648488.1:c.293+19del	ENSP00000498079.1:n.293+19del
ENST00000649823.1:n.561+19del
ENST00000649868.1:c.*52+19del	ENSP00000497548.1:n.*52+19del
ENST00000650101.1:c.275+19del	ENSP00000496970.1:n.275+19del
ENST00000650307.1:n.1170+19del
ENST00000652429.1:c.344+19del MANE Select	ENSP00000498786.1:n.344+19del
ENST00000278715.7:c.344+19del	ENSP00000278715.3:n.344+19del
ENST00000392841.1:c.293+19del	ENSP00000376584.1:n.293+19del
ENST00000442944.6:c.293+19del	ENSP00000392041.2:n.293+19del
ENST00000534956.1:n.260+19del
ENST00000535253.5:c.293+19del	ENSP00000442079.1:n.293+19del
ENST00000535793.5:c.*239+19del	ENSP00000439904.1:n.*239+19del
ENST00000536813.5:c.326+19del	ENSP00000438726.1:n.326+19del
ENST00000537841.5:c.293+19del	ENSP00000444730.1:n.293+19del
ENST00000539986.5:c.293+19del	ENSP00000440092.1:n.293+19del
ENST00000542044.5:n.789+19del
ENST00000542345.5:n.482+19del
ENST00000542729.5:c.293+19del	ENSP00000443058.1:n.293+19del
ENST00000542822.5:c.*280+19del	ENSP00000444817.1:n.*280+19del
ENST00000543090.5:c.290+19del	ENSP00000445429.1:n.290+19del
ENST00000543543.5:n.579+19del
ENST00000543821.5:n.505+4del
ENST00000544360.5:n.312+19del
ENST00000544387.5:c.344+19del	ENSP00000438424.1:n.344+19del
ENST00000545621.5:c.*239+19del	ENSP00000444849.1:n.*239+19del
ENST00000546226.5:n.422del
ENST00000546302.5:c.267-211del	ENSP00000445599.1:n.267-211del
NM_000190.3:c.344+19del	NP_000181.2:n.344+19del
NM_001024382.1:c.293+19del	NP_001019553.1:n.293+19del
NM_001258208.1:c.344+19del	NP_001245137.1:n.344+19del
NM_001258209.1:c.293+19del	NP_001245138.1:n.293+19del
XM_005271531.1:c.293+19del	XP_005271588.1:n.293+19del
XM_005271532.1:c.293+19del	XP_005271589.1:n.293+19del
XM_005271533.2:c.290+19del	XP_005271590.1:n.290+19del
XM_011542796.1:c.179+19del	XP_011541098.1:n.179+19del
NM_000190.4:c.344+19del MANE Select	NP_000181.2:n.344+19del
NM_001024382.2:c.293+19del	NP_001019553.1:n.293+19del
XM_005271533.3:c.290+19del	XP_005271590.1:n.290+19del
XM_017017629.1:c.293+19del	XP_016873118.1:n.293+19del
XM_024448460.1:c.290+19del	XP_024304228.1:n.290+19del
NM_001258208.2:c.344+19del	NP_001245137.1:n.344+19del
NM_001258209.2:c.293+19del	NP_001245138.1:n.293+19del