Canonical Allele Identifier: CA382894166

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118962135A>C (hg19) ; chr11:g.119091425A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119091425A>C , CM000673.2:g.119091425A>C	GRCh38
NC_000011.9:g.118962135A>C , CM000673.1:g.118962135A>C	GRCh37
NC_000011.8:g.118467345A>C	NCBI36
NG_008093.1:g.11549A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.346A>C	ENSP00000509288.1:p.Asn116His
ENST00000686690.1:n.1361A>C
ENST00000691144.1:n.2252A>C
ENST00000691249.1:n.1095A>C
ENST00000442944.7:c.493A>C	ENSP00000392041.3:p.Asn165His
ENST00000534956.2:n.448-436A>C
ENST00000536813.6:c.460A>C	ENSP00000438726.2:p.Asn154His
ENST00000546302.6:c.433A>C	ENSP00000445599.1:p.Asn145His
ENST00000640813.1:c.448-436A>C	ENSP00000491061.1:n.448-436A>C
ENST00000648026.1:c.493-436A>C	ENSP00000498044.1:n.493-436A>C
ENST00000648374.1:c.460A>C	ENSP00000497255.1:p.Asn154His
ENST00000648488.1:c.*85+169A>C	ENSP00000498079.1:n.*85+169A>C
ENST00000649823.1:n.728A>C
ENST00000649868.1:c.*207-436A>C	ENSP00000497548.1:n.*207-436A>C
ENST00000650101.1:c.442A>C	ENSP00000496970.1:p.Asn148His
ENST00000650307.1:n.1337A>C
ENST00000652429.1:c.511A>C MANE Select	ENSP00000498786.1:p.Asn171His
ENST00000278715.7:c.511A>C	ENSP00000278715.3:p.Asn171His
ENST00000392841.1:c.460A>C	ENSP00000376584.1:p.Asn154His
ENST00000442944.6:c.460A>C	ENSP00000392041.2:p.Asn154His
ENST00000534956.1:n.415-436A>C
ENST00000535253.5:c.460A>C	ENSP00000442079.1:p.Asn154His
ENST00000535793.5:c.*406A>C	ENSP00000439904.1:n.*406A>C
ENST00000537841.5:c.460A>C	ENSP00000444730.1:p.Asn154His
ENST00000539986.5:c.460A>C	ENSP00000440092.1:p.Asn154His
ENST00000542044.5:n.956A>C
ENST00000542345.5:n.649A>C
ENST00000542729.5:c.460A>C	ENSP00000443058.1:p.Asn154His
ENST00000542822.5:c.*447A>C	ENSP00000444817.1:n.*447A>C
ENST00000543090.5:c.457A>C	ENSP00000445429.1:p.Asn153His
ENST00000543543.5:n.746A>C
ENST00000544360.5:n.479A>C
ENST00000544387.5:c.511A>C	ENSP00000438424.1:p.Asn171His
ENST00000545621.5:c.*406A>C	ENSP00000444849.1:n.*406A>C
ENST00000546226.5:n.799A>C
ENST00000546302.5:c.433A>C	ENSP00000445599.1:p.Asn145His
NM_000190.3:c.511A>C	NP_000181.2:p.Asn171His
NM_001024382.1:c.460A>C	NP_001019553.1:p.Asn154His
NM_001258208.1:c.511A>C	NP_001245137.1:p.Asn171His
NM_001258209.1:c.460A>C	NP_001245138.1:p.Asn154His
XM_005271531.1:c.460A>C	XP_005271588.1:p.Asn154His
XM_005271532.1:c.460A>C	XP_005271589.1:p.Asn154His
XM_005271533.2:c.457A>C	XP_005271590.1:p.Asn153His
XM_011542796.1:c.346A>C	XP_011541098.1:p.Asn116His
NM_000190.4:c.511A>C MANE Select	NP_000181.2:p.Asn171His
NM_001024382.2:c.460A>C	NP_001019553.1:p.Asn154His
XM_005271533.3:c.457A>C	XP_005271590.1:p.Asn153His
XM_017017629.1:c.460A>C	XP_016873118.1:p.Asn154His
XM_024448460.1:c.457A>C	XP_024304228.1:p.Asn153His
NM_001258208.2:c.511A>C	NP_001245137.1:p.Asn171His
NM_001258209.2:c.460A>C	NP_001245138.1:p.Asn154His