Canonical Allele Identifier: CA382898314

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963487C>G (hg19) ; chr11:g.119092777C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092777C>G , CM000673.2:g.119092777C>G	GRCh38
NC_000011.9:g.118963487C>G , CM000673.1:g.118963487C>G	GRCh37
NC_000011.8:g.118468697C>G	NCBI36
NG_008093.1:g.12901C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.626C>G	ENSP00000509288.1:p.Pro209Arg
ENST00000691144.1:n.3006C>G
ENST00000691249.1:n.1615C>G
ENST00000442944.7:c.773C>G	ENSP00000392041.3:p.Pro258Arg
ENST00000640813.1:c.*28C>G	ENSP00000491061.1:n.*28C>G
ENST00000648026.1:c.685C>G	ENSP00000498044.1:n.685C>G
ENST00000648374.1:c.740C>G	ENSP00000497255.1:p.Pro247Arg
ENST00000649823.1:n.1248C>G
ENST00000650101.1:c.722C>G	ENSP00000496970.1:p.Pro241Arg
ENST00000650307.1:n.1617C>G
ENST00000652429.1:c.791C>G MANE Select	ENSP00000498786.1:p.Pro264Arg
ENST00000278715.7:c.791C>G	ENSP00000278715.3:p.Pro264Arg
ENST00000392841.1:c.740C>G	ENSP00000376584.1:p.Pro247Arg
ENST00000442944.6:c.740C>G	ENSP00000392041.2:p.Pro247Arg
ENST00000537841.5:c.740C>G	ENSP00000444730.1:p.Pro247Arg
ENST00000539045.1:n.167C>G
ENST00000542044.5:n.1236C>G
ENST00000542729.5:c.620C>G	ENSP00000443058.1:p.Pro207Arg
ENST00000543090.5:c.698C>G	ENSP00000445429.1:p.Pro233Arg
ENST00000543543.5:n.1266C>G
ENST00000544182.1:n.1240C>G
ENST00000544387.5:c.671C>G	ENSP00000438424.1:p.Pro224Arg
ENST00000546226.5:n.1553C>G
NM_000190.3:c.791C>G	NP_000181.2:p.Pro264Arg
NM_001024382.1:c.740C>G	NP_001019553.1:p.Pro247Arg
NM_001258208.1:c.671C>G	NP_001245137.1:p.Pro224Arg
NM_001258209.1:c.620C>G	NP_001245138.1:p.Pro207Arg
XM_005271531.1:c.740C>G	XP_005271588.1:p.Pro247Arg
XM_005271532.1:c.740C>G	XP_005271589.1:p.Pro247Arg
XM_005271533.2:c.737C>G	XP_005271590.1:p.Pro246Arg
XM_011542796.1:c.626C>G	XP_011541098.1:p.Pro209Arg
NM_000190.4:c.791C>G MANE Select	NP_000181.2:p.Pro264Arg
NM_001024382.2:c.740C>G	NP_001019553.1:p.Pro247Arg
XM_005271533.3:c.737C>G	XP_005271590.1:p.Pro246Arg
XM_017017629.1:c.740C>G	XP_016873118.1:p.Pro247Arg
XM_024448460.1:c.617C>G	XP_024304228.1:p.Pro206Arg
NM_001258208.2:c.671C>G	NP_001245137.1:p.Pro224Arg
NM_001258209.2:c.620C>G	NP_001245138.1:p.Pro207Arg