Canonical Allele Identifier: CA2003791326

Gene: HMBS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092350_119092351delinsCG , CM000673.2:g.119092350_119092351delinsCG	GRCh38
NC_000011.9:g.118963060_118963061delinsCG , CM000673.1:g.118963060_118963061delinsCG	GRCh37
NC_000011.8:g.118468270_118468271delinsCG	NCBI36
NG_008093.1:g.12474_12475delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.487-54_487-53delinsCG	ENSP00000509288.1:n.487-54_487-53delinsCG
ENST00000691144.1:n.2579_2580delinsCG
ENST00000691249.1:n.1422_1423delinsCG
ENST00000442944.7:c.634-54_634-53delinsCG	ENSP00000392041.3:n.634-54_634-53delinsCG
ENST00000536813.6:c.601-54_601-53delinsCG	ENSP00000438726.2:n.601-54_601-53delinsCG
ENST00000640813.1:c.462-54_462-53delinsCG	ENSP00000491061.1:n.462-54_462-53delinsCG
ENST00000648026.1:c.546-54_546-53delinsCG	ENSP00000498044.1:n.546-54_546-53delinsCG
ENST00000648374.1:c.601-54_601-53delinsCG	ENSP00000497255.1:n.601-54_601-53delinsCG
ENST00000649823.1:n.1055_1056delinsCG
ENST00000650101.1:c.583-54_583-53delinsCG	ENSP00000496970.1:n.583-54_583-53delinsCG
ENST00000650307.1:n.1478-54_1478-53delinsCG
ENST00000652429.1:c.652-54_652-53delinsCG MANE Select	ENSP00000498786.1:n.652-54_652-53delinsCG
ENST00000278715.7:c.652-54_652-53delinsCG	ENSP00000278715.3:n.652-54_652-53delinsCG
ENST00000392841.1:c.601-54_601-53delinsCG	ENSP00000376584.1:n.601-54_601-53delinsCG
ENST00000442944.6:c.601-54_601-53delinsCG	ENSP00000392041.2:n.601-54_601-53delinsCG
ENST00000537841.5:c.601-54_601-53delinsCG	ENSP00000444730.1:n.601-54_601-53delinsCG
ENST00000542044.5:n.1097-54_1097-53delinsCG
ENST00000542729.5:c.600+187_600+188delinsCG	ENSP00000443058.1:n.600+187_600+188delinsCG
ENST00000543090.5:c.559-54_559-53delinsCG	ENSP00000445429.1:n.559-54_559-53delinsCG
ENST00000543543.5:n.1073_1074delinsCG
ENST00000544182.1:n.813_814delinsCG
ENST00000544387.5:c.651+187_651+188delinsCG	ENSP00000438424.1:n.651+187_651+188delinsCG
ENST00000545621.5:c.*733_*734delinsCG	ENSP00000444849.1:n.*733_*734delinsCG
ENST00000546226.5:n.1126_1127delinsCG
NM_000190.3:c.652-54_652-53delinsCG	NP_000181.2:n.652-54_652-53delinsCG
NM_001024382.1:c.601-54_601-53delinsCG	NP_001019553.1:n.601-54_601-53delinsCG
NM_001258208.1:c.651+187_651+188delinsCG	NP_001245137.1:n.651+187_651+188delinsCG
NM_001258209.1:c.600+187_600+188delinsCG	NP_001245138.1:n.600+187_600+188delinsCG
XM_005271531.1:c.601-54_601-53delinsCG	XP_005271588.1:n.601-54_601-53delinsCG
XM_005271532.1:c.601-54_601-53delinsCG	XP_005271589.1:n.601-54_601-53delinsCG
XM_005271533.2:c.598-54_598-53delinsCG	XP_005271590.1:n.598-54_598-53delinsCG
XM_011542796.1:c.487-54_487-53delinsCG	XP_011541098.1:n.487-54_487-53delinsCG
NM_000190.4:c.652-54_652-53delinsCG MANE Select	NP_000181.2:n.652-54_652-53delinsCG
NM_001024382.2:c.601-54_601-53delinsCG	NP_001019553.1:n.601-54_601-53delinsCG
XM_005271533.3:c.598-54_598-53delinsCG	XP_005271590.1:n.598-54_598-53delinsCG
XM_017017629.1:c.601-54_601-53delinsCG	XP_016873118.1:n.601-54_601-53delinsCG
XM_024448460.1:c.597+187_597+188delinsCG	XP_024304228.1:n.597+187_597+188delinsCG
NM_001258208.2:c.651+187_651+188delinsCG	NP_001245137.1:n.651+187_651+188delinsCG
NM_001258209.2:c.600+187_600+188delinsCG	NP_001245138.1:n.600+187_600+188delinsCG