Canonical Allele Identifier: CA2003793003

Gene: HMBS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119093041_119093042delinsAG , CM000673.2:g.119093041_119093042delinsAG	GRCh38
NC_000011.9:g.118963751_118963752delinsAG , CM000673.1:g.118963751_118963752delinsAG	GRCh37
NC_000011.8:g.118468961_118468962delinsAG	NCBI36
NG_008093.1:g.13165_13166delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.747+20_747+21delinsAG	ENSP00000509288.1:n.747+20_747+21delinsAG
ENST00000691144.1:n.3127+20_3127+21delinsAG
ENST00000691249.1:n.1736+20_1736+21delinsAG
ENST00000442944.7:c.894+20_894+21delinsAG	ENSP00000392041.3:n.894+20_894+21delinsAG
ENST00000640813.1:c.*149+20_*149+21delinsAG	ENSP00000491061.1:n.*149+20_*149+21delinsAG
ENST00000648026.1:c.806+20_806+21delinsAG	ENSP00000498044.1:n.806+20_806+21delinsAG
ENST00000648374.1:c.861+20_861+21delinsAG	ENSP00000497255.1:n.861+20_861+21delinsAG
ENST00000650101.1:c.843+20_843+21delinsAG	ENSP00000496970.1:n.843+20_843+21delinsAG
ENST00000650307.1:n.1738+20_1738+21delinsAG
ENST00000652429.1:c.912+20_912+21delinsAG MANE Select	ENSP00000498786.1:n.912+20_912+21delinsAG
ENST00000278715.7:c.912+20_912+21delinsAG	ENSP00000278715.3:n.912+20_912+21delinsAG
ENST00000392841.1:c.861+20_861+21delinsAG	ENSP00000376584.1:n.861+20_861+21delinsAG
ENST00000442944.6:c.861+20_861+21delinsAG	ENSP00000392041.2:n.861+20_861+21delinsAG
ENST00000537841.5:c.861+20_861+21delinsAG	ENSP00000444730.1:n.861+20_861+21delinsAG
ENST00000539045.1:n.411+20_411+21delinsAG
ENST00000542044.5:n.1357+20_1357+21delinsAG
ENST00000542729.5:c.741+20_741+21delinsAG	ENSP00000443058.1:n.741+20_741+21delinsAG
ENST00000543090.5:c.819+20_819+21delinsAG	ENSP00000445429.1:n.819+20_819+21delinsAG
ENST00000543543.5:n.1387+20_1387+21delinsAG
ENST00000544182.1:n.1361+20_1361+21delinsAG
ENST00000544387.5:c.792+20_792+21delinsAG	ENSP00000438424.1:n.792+20_792+21delinsAG
ENST00000546226.5:n.1674+20_1674+21delinsAG
NM_000190.3:c.912+20_912+21delinsAG	NP_000181.2:n.912+20_912+21delinsAG
NM_001024382.1:c.861+20_861+21delinsAG	NP_001019553.1:n.861+20_861+21delinsAG
NM_001258208.1:c.792+20_792+21delinsAG	NP_001245137.1:n.792+20_792+21delinsAG
NM_001258209.1:c.741+20_741+21delinsAG	NP_001245138.1:n.741+20_741+21delinsAG
XM_005271531.1:c.861+20_861+21delinsAG	XP_005271588.1:n.861+20_861+21delinsAG
XM_005271532.1:c.861+20_861+21delinsAG	XP_005271589.1:n.861+20_861+21delinsAG
XM_005271533.2:c.858+20_858+21delinsAG	XP_005271590.1:n.858+20_858+21delinsAG
XM_011542796.1:c.747+20_747+21delinsAG	XP_011541098.1:n.747+20_747+21delinsAG
NM_000190.4:c.912+20_912+21delinsAG MANE Select	NP_000181.2:n.912+20_912+21delinsAG
NM_001024382.2:c.861+20_861+21delinsAG	NP_001019553.1:n.861+20_861+21delinsAG
XM_005271533.3:c.858+20_858+21delinsAG	XP_005271590.1:n.858+20_858+21delinsAG
XM_017017629.1:c.861+20_861+21delinsAG	XP_016873118.1:n.861+20_861+21delinsAG
XM_024448460.1:c.738+20_738+21delinsAG	XP_024304228.1:n.738+20_738+21delinsAG
NM_001258208.2:c.792+20_792+21delinsAG	NP_001245137.1:n.792+20_792+21delinsAG
NM_001258209.2:c.741+20_741+21delinsAG	NP_001245138.1:n.741+20_741+21delinsAG