Canonical Allele Identifier: CA382897455

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963154T>A (hg19) ; chr11:g.119092444T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092444T>A , CM000673.2:g.119092444T>A	GRCh38
NC_000011.9:g.118963154T>A , CM000673.1:g.118963154T>A	GRCh37
NC_000011.8:g.118468364T>A	NCBI36
NG_008093.1:g.12568T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.527T>A	ENSP00000509288.1:p.Ile176Asn
ENST00000691144.1:n.2673T>A
ENST00000691249.1:n.1516T>A
ENST00000442944.7:c.674T>A	ENSP00000392041.3:p.Ile225Asn
ENST00000536813.6:c.641T>A	ENSP00000438726.2:p.Ile214Asn
ENST00000640813.1:c.502T>A	ENSP00000491061.1:p.Ser168Thr
ENST00000648026.1:c.586T>A	ENSP00000498044.1:p.Ser196Thr
ENST00000648374.1:c.641T>A	ENSP00000497255.1:p.Ile214Asn
ENST00000649823.1:n.1149T>A
ENST00000650101.1:c.623T>A	ENSP00000496970.1:p.Ile208Asn
ENST00000650307.1:n.1518T>A
ENST00000652429.1:c.692T>A MANE Select	ENSP00000498786.1:p.Ile231Asn
ENST00000278715.7:c.692T>A	ENSP00000278715.3:p.Ile231Asn
ENST00000392841.1:c.641T>A	ENSP00000376584.1:p.Ile214Asn
ENST00000442944.6:c.641T>A	ENSP00000392041.2:p.Ile214Asn
ENST00000537841.5:c.641T>A	ENSP00000444730.1:p.Ile214Asn
ENST00000542044.5:n.1137T>A
ENST00000542729.5:c.600+281T>A	ENSP00000443058.1:n.600+281T>A
ENST00000543090.5:c.599T>A	ENSP00000445429.1:p.Ile200Asn
ENST00000543543.5:n.1167T>A
ENST00000544182.1:n.907T>A
ENST00000544387.5:c.651+281T>A	ENSP00000438424.1:n.651+281T>A
ENST00000545621.5:c.*827T>A	ENSP00000444849.1:n.*827T>A
ENST00000546226.5:n.1220T>A
NM_000190.3:c.692T>A	NP_000181.2:p.Ile231Asn
NM_001024382.1:c.641T>A	NP_001019553.1:p.Ile214Asn
NM_001258208.1:c.651+281T>A	NP_001245137.1:n.651+281T>A
NM_001258209.1:c.600+281T>A	NP_001245138.1:n.600+281T>A
XM_005271531.1:c.641T>A	XP_005271588.1:p.Ile214Asn
XM_005271532.1:c.641T>A	XP_005271589.1:p.Ile214Asn
XM_005271533.2:c.638T>A	XP_005271590.1:p.Ile213Asn
XM_011542796.1:c.527T>A	XP_011541098.1:p.Ile176Asn
NM_000190.4:c.692T>A MANE Select	NP_000181.2:p.Ile231Asn
NM_001024382.2:c.641T>A	NP_001019553.1:p.Ile214Asn
XM_005271533.3:c.638T>A	XP_005271590.1:p.Ile213Asn
XM_017017629.1:c.641T>A	XP_016873118.1:p.Ile214Asn
XM_024448460.1:c.597+281T>A	XP_024304228.1:n.597+281T>A
NM_001258208.2:c.651+281T>A	NP_001245137.1:n.651+281T>A
NM_001258209.2:c.600+281T>A	NP_001245138.1:n.600+281T>A