Canonical Allele Identifier: CA382899974

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963956T>C (hg19) ; chr11:g.119093246T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119093246T>C , CM000673.2:g.119093246T>C	GRCh38
NC_000011.9:g.118963956T>C , CM000673.1:g.118963956T>C	GRCh37
NC_000011.8:g.118469166T>C	NCBI36
NG_008093.1:g.13370T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.884T>C	ENSP00000509288.1:p.Ile295Thr
ENST00000691144.1:n.3264T>C
ENST00000691249.1:n.1873T>C
ENST00000442944.7:c.1031T>C	ENSP00000392041.3:p.Ile344Thr
ENST00000640813.1:c.*286T>C	ENSP00000491061.1:n.*286T>C
ENST00000648026.1:c.943T>C	ENSP00000498044.1:n.943T>C
ENST00000648374.1:c.998T>C	ENSP00000497255.1:p.Ile333Thr
ENST00000650101.1:c.980T>C	ENSP00000496970.1:p.Ile327Thr
ENST00000650307.1:n.1875T>C
ENST00000652429.1:c.1049T>C MANE Select	ENSP00000498786.1:p.Ile350Thr
ENST00000278715.7:c.1049T>C	ENSP00000278715.3:p.Ile350Thr
ENST00000392841.1:c.998T>C	ENSP00000376584.1:p.Ile333Thr
ENST00000442944.6:c.998T>C	ENSP00000392041.2:p.Ile333Thr
ENST00000537841.5:c.998T>C	ENSP00000444730.1:p.Ile333Thr
ENST00000539045.1:n.548T>C
ENST00000542044.5:n.1494T>C
ENST00000542729.5:c.878T>C	ENSP00000443058.1:p.Ile293Thr
ENST00000543090.5:c.956T>C	ENSP00000445429.1:p.Ile319Thr
ENST00000543543.5:n.1524T>C
ENST00000544182.1:n.1498T>C
ENST00000544387.5:c.929T>C	ENSP00000438424.1:p.Ile310Thr
ENST00000546226.5:n.1811T>C
NM_000190.3:c.1049T>C	NP_000181.2:p.Ile350Thr
NM_001024382.1:c.998T>C	NP_001019553.1:p.Ile333Thr
NM_001258208.1:c.929T>C	NP_001245137.1:p.Ile310Thr
NM_001258209.1:c.878T>C	NP_001245138.1:p.Ile293Thr
XM_005271531.1:c.998T>C	XP_005271588.1:p.Ile333Thr
XM_005271532.1:c.998T>C	XP_005271589.1:p.Ile333Thr
XM_005271533.2:c.995T>C	XP_005271590.1:p.Ile332Thr
XM_011542796.1:c.884T>C	XP_011541098.1:p.Ile295Thr
NM_000190.4:c.1049T>C MANE Select	NP_000181.2:p.Ile350Thr
NM_001024382.2:c.998T>C	NP_001019553.1:p.Ile333Thr
XM_005271533.3:c.995T>C	XP_005271590.1:p.Ile332Thr
XM_017017629.1:c.998T>C	XP_016873118.1:p.Ile333Thr
XM_024448460.1:c.875T>C	XP_024304228.1:p.Ile292Thr
NM_001258208.2:c.929T>C	NP_001245137.1:p.Ile310Thr
NM_001258209.2:c.878T>C	NP_001245138.1:p.Ile293Thr