Canonical Allele Identifier: CA2003792909

Gene: HMBS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119093008_119093009delinsAT , CM000673.2:g.119093008_119093009delinsAT	GRCh38
NC_000011.9:g.118963718_118963719delinsAT , CM000673.1:g.118963718_118963719delinsAT	GRCh37
NC_000011.8:g.118468928_118468929delinsAT	NCBI36
NG_008093.1:g.13132_13133delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.734_735delinsAT	ENSP00000509288.1:p.His245=
ENST00000691144.1:n.3114_3115delinsAT
ENST00000691249.1:n.1723_1724delinsAT
ENST00000442944.7:c.881_882delinsAT	ENSP00000392041.3:p.His294=
ENST00000640813.1:c.*136_*137delinsAT	ENSP00000491061.1:n.*136_*137delinsAT
ENST00000648026.1:c.793_794delinsAT	ENSP00000498044.1:n.793_794delinsAT
ENST00000648374.1:c.848_849delinsAT	ENSP00000497255.1:p.His283=
ENST00000650101.1:c.830_831delinsAT	ENSP00000496970.1:p.His277=
ENST00000650307.1:n.1725_1726delinsAT
ENST00000652429.1:c.899_900delinsAT MANE Select	ENSP00000498786.1:p.His300=
ENST00000278715.7:c.899_900delinsAT	ENSP00000278715.3:p.His300=
ENST00000392841.1:c.848_849delinsAT	ENSP00000376584.1:p.His283=
ENST00000442944.6:c.848_849delinsAT	ENSP00000392041.2:p.His283=
ENST00000537841.5:c.848_849delinsAT	ENSP00000444730.1:p.His283=
ENST00000539045.1:n.398_399delinsAT
ENST00000542044.5:n.1344_1345delinsAT
ENST00000542729.5:c.728_729delinsAT	ENSP00000443058.1:p.His243=
ENST00000543090.5:c.806_807delinsAT	ENSP00000445429.1:p.His269=
ENST00000543543.5:n.1374_1375delinsAT
ENST00000544182.1:n.1348_1349delinsAT
ENST00000544387.5:c.779_780delinsAT	ENSP00000438424.1:p.His260=
ENST00000546226.5:n.1661_1662delinsAT
NM_000190.3:c.899_900delinsAT	NP_000181.2:p.His300=
NM_001024382.1:c.848_849delinsAT	NP_001019553.1:p.His283=
NM_001258208.1:c.779_780delinsAT	NP_001245137.1:p.His260=
NM_001258209.1:c.728_729delinsAT	NP_001245138.1:p.His243=
XM_005271531.1:c.848_849delinsAT	XP_005271588.1:p.His283=
XM_005271532.1:c.848_849delinsAT	XP_005271589.1:p.His283=
XM_005271533.2:c.845_846delinsAT	XP_005271590.1:p.His282=
XM_011542796.1:c.734_735delinsAT	XP_011541098.1:p.His245=
NM_000190.4:c.899_900delinsAT MANE Select	NP_000181.2:p.His300=
NM_001024382.2:c.848_849delinsAT	NP_001019553.1:p.His283=
XM_005271533.3:c.845_846delinsAT	XP_005271590.1:p.His282=
XM_017017629.1:c.848_849delinsAT	XP_016873118.1:p.His283=
XM_024448460.1:c.725_726delinsAT	XP_024304228.1:p.His242=
NM_001258208.2:c.779_780delinsAT	NP_001245137.1:p.His260=
NM_001258209.2:c.728_729delinsAT	NP_001245138.1:p.His243=