Canonical Allele Identifier: CA382890495

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118960400C>G (hg19) ; chr11:g.119089690C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119089690C>G , CM000673.2:g.119089690C>G	GRCh38
NC_000011.9:g.118960400C>G , CM000673.1:g.118960400C>G	GRCh37
NC_000011.8:g.118465610C>G	NCBI36
NG_008093.1:g.9814C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.109C>G	ENSP00000509288.1:p.Leu37Val
ENST00000686690.1:n.895C>G
ENST00000691144.1:n.2015C>G
ENST00000691249.1:n.858C>G
ENST00000442944.7:c.256C>G	ENSP00000392041.3:p.Leu86Val
ENST00000534956.2:n.223C>G
ENST00000536813.6:c.223C>G	ENSP00000438726.2:p.Leu75Val
ENST00000546302.6:c.267-300C>G	ENSP00000445599.1:n.267-300C>G
ENST00000640813.1:c.223C>G	ENSP00000491061.1:p.Leu75Val
ENST00000648026.1:c.268C>G	ENSP00000498044.1:p.Leu90Val
ENST00000648374.1:c.223C>G	ENSP00000497255.1:p.Leu75Val
ENST00000648488.1:c.223C>G	ENSP00000498079.1:p.Leu75Val
ENST00000649823.1:n.491C>G
ENST00000649868.1:c.129C>G	ENSP00000497548.1:p.Thr43=
ENST00000650101.1:c.205C>G	ENSP00000496970.1:p.Leu69Val
ENST00000650307.1:n.1100C>G
ENST00000652429.1:c.274C>G MANE Select	ENSP00000498786.1:p.Leu92Val
ENST00000278715.7:c.274C>G	ENSP00000278715.3:p.Leu92Val
ENST00000392841.1:c.223C>G	ENSP00000376584.1:p.Leu75Val
ENST00000442944.6:c.223C>G	ENSP00000392041.2:p.Leu75Val
ENST00000534956.1:n.190C>G
ENST00000535253.5:c.223C>G	ENSP00000442079.1:p.Leu75Val
ENST00000535793.5:c.*169C>G	ENSP00000439904.1:n.*169C>G
ENST00000536185.5:n.392C>G
ENST00000536813.5:c.256C>G	ENSP00000438726.1:p.Leu86Val
ENST00000537841.5:c.223C>G	ENSP00000444730.1:p.Leu75Val
ENST00000539986.5:c.223C>G	ENSP00000440092.1:p.Leu75Val
ENST00000542044.5:n.719C>G
ENST00000542345.5:n.412C>G
ENST00000542729.5:c.223C>G	ENSP00000443058.1:p.Leu75Val
ENST00000542822.5:c.*210C>G	ENSP00000444817.1:n.*210C>G
ENST00000543090.5:c.220C>G	ENSP00000445429.1:p.Leu74Val
ENST00000543543.5:n.509C>G
ENST00000543821.5:n.420C>G
ENST00000544360.5:n.242C>G
ENST00000544387.5:c.274C>G	ENSP00000438424.1:p.Leu92Val
ENST00000545621.5:c.*169C>G	ENSP00000444849.1:n.*169C>G
ENST00000546226.5:n.333C>G
ENST00000546302.5:c.267-300C>G	ENSP00000445599.1:n.267-300C>G
NM_000190.3:c.274C>G	NP_000181.2:p.Leu92Val
NM_001024382.1:c.223C>G	NP_001019553.1:p.Leu75Val
NM_001258208.1:c.274C>G	NP_001245137.1:p.Leu92Val
NM_001258209.1:c.223C>G	NP_001245138.1:p.Leu75Val
XM_005271531.1:c.223C>G	XP_005271588.1:p.Leu75Val
XM_005271532.1:c.223C>G	XP_005271589.1:p.Leu75Val
XM_005271533.2:c.220C>G	XP_005271590.1:p.Leu74Val
XM_011542796.1:c.109C>G	XP_011541098.1:p.Leu37Val
NM_000190.4:c.274C>G MANE Select	NP_000181.2:p.Leu92Val
NM_001024382.2:c.223C>G	NP_001019553.1:p.Leu75Val
XM_005271533.3:c.220C>G	XP_005271590.1:p.Leu74Val
XM_017017629.1:c.223C>G	XP_016873118.1:p.Leu75Val
XM_024448460.1:c.220C>G	XP_024304228.1:p.Leu74Val
NM_001258208.2:c.274C>G	NP_001245137.1:p.Leu92Val
NM_001258209.2:c.223C>G	NP_001245138.1:p.Leu75Val