Canonical Allele Identifier: CA382894715

Gene: HMBS

Linked Data

• gnomAD v4: 11-119091492-T-C
• MyVariant Identifiers: chr11:g.118962202T>C (hg19) ; chr11:g.119091492T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119091492T>C , CM000673.2:g.119091492T>C	GRCh38
NC_000011.9:g.118962202T>C , CM000673.1:g.118962202T>C	GRCh37
NC_000011.8:g.118467412T>C	NCBI36
NG_008093.1:g.11616T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.413T>C	ENSP00000509288.1:p.Leu138Pro
ENST00000686690.1:n.1428T>C
ENST00000691144.1:n.2319T>C
ENST00000691249.1:n.1162T>C
ENST00000442944.7:c.560T>C	ENSP00000392041.3:p.Leu187Pro
ENST00000534956.2:n.448-369T>C
ENST00000536813.6:c.527T>C	ENSP00000438726.2:p.Leu176Pro
ENST00000546302.6:c.500T>C	ENSP00000445599.1:p.Leu167Pro
ENST00000640813.1:c.448-369T>C	ENSP00000491061.1:n.448-369T>C
ENST00000648026.1:c.493-369T>C	ENSP00000498044.1:n.493-369T>C
ENST00000648374.1:c.527T>C	ENSP00000497255.1:p.Leu176Pro
ENST00000648488.1:c.*85+236T>C	ENSP00000498079.1:n.*85+236T>C
ENST00000649823.1:n.795T>C
ENST00000649868.1:c.*207-369T>C	ENSP00000497548.1:n.*207-369T>C
ENST00000650101.1:c.509T>C	ENSP00000496970.1:p.Leu170Pro
ENST00000650307.1:n.1404T>C
ENST00000652429.1:c.578T>C MANE Select	ENSP00000498786.1:p.Leu193Pro
ENST00000278715.7:c.578T>C	ENSP00000278715.3:p.Leu193Pro
ENST00000392841.1:c.527T>C	ENSP00000376584.1:p.Leu176Pro
ENST00000442944.6:c.527T>C	ENSP00000392041.2:p.Leu176Pro
ENST00000534956.1:n.415-369T>C
ENST00000535253.5:c.527T>C	ENSP00000442079.1:p.Leu176Pro
ENST00000535793.5:c.*473T>C	ENSP00000439904.1:n.*473T>C
ENST00000537841.5:c.527T>C	ENSP00000444730.1:p.Leu176Pro
ENST00000539986.5:c.527T>C	ENSP00000440092.1:p.Leu176Pro
ENST00000542044.5:n.1023T>C
ENST00000542345.5:n.716T>C
ENST00000542729.5:c.527T>C	ENSP00000443058.1:p.Leu176Pro
ENST00000542822.5:c.*514T>C	ENSP00000444817.1:n.*514T>C
ENST00000543090.5:c.524T>C	ENSP00000445429.1:p.Leu175Pro
ENST00000543543.5:n.813T>C
ENST00000544360.5:n.546T>C
ENST00000544387.5:c.578T>C	ENSP00000438424.1:p.Leu193Pro
ENST00000545621.5:c.*473T>C	ENSP00000444849.1:n.*473T>C
ENST00000546226.5:n.866T>C
ENST00000546302.5:c.500T>C	ENSP00000445599.1:p.Leu167Pro
NM_000190.3:c.578T>C	NP_000181.2:p.Leu193Pro
NM_001024382.1:c.527T>C	NP_001019553.1:p.Leu176Pro
NM_001258208.1:c.578T>C	NP_001245137.1:p.Leu193Pro
NM_001258209.1:c.527T>C	NP_001245138.1:p.Leu176Pro
XM_005271531.1:c.527T>C	XP_005271588.1:p.Leu176Pro
XM_005271532.1:c.527T>C	XP_005271589.1:p.Leu176Pro
XM_005271533.2:c.524T>C	XP_005271590.1:p.Leu175Pro
XM_011542796.1:c.413T>C	XP_011541098.1:p.Leu138Pro
NM_000190.4:c.578T>C MANE Select	NP_000181.2:p.Leu193Pro
NM_001024382.2:c.527T>C	NP_001019553.1:p.Leu176Pro
XM_005271533.3:c.524T>C	XP_005271590.1:p.Leu175Pro
XM_017017629.1:c.527T>C	XP_016873118.1:p.Leu176Pro
XM_024448460.1:c.524T>C	XP_024304228.1:p.Leu175Pro
NM_001258208.2:c.578T>C	NP_001245137.1:p.Leu193Pro
NM_001258209.2:c.527T>C	NP_001245138.1:p.Leu176Pro