Canonical Allele Identifier: CA6313845

Gene: HMBS

Linked Data

• dbSNP Id: rs782654123
• ExAC: 11:118955817 G / GTGCCTGT
• MyVariant Identifiers: chr11:g.118955817_118955818insTGCCTGT (hg19) ; chr11:g.119085107_119085108insTGCCTGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119085107_119085108insTGCCTGT , CM000673.2:g.119085107_119085108insTGCCTGT	GRCh38
NC_000011.9:g.118955817_118955818insTGCCTGT , CM000673.1:g.118955817_118955818insTGCCTGT	GRCh37
NC_000011.8:g.118461027_118461028insTGCCTGT	NCBI36
NG_008093.1:g.5231_5232insTGCCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442944.7:c.33+41_33+42insTGCCTGT	ENSP00000392041.3:n.33+41_33+42insTGCCTGT
ENST00000534956.2:n.36+41_36+42insTGCCTGT
ENST00000536813.6:c.-102+41_-102+42insTGCCTGT	ENSP00000438726.2:n.-102+41_-102+42insTGCCTGT
ENST00000546302.6:c.33+41_33+42insTGCCTGT	ENSP00000445599.1:n.33+41_33+42insTGCCTGT
ENST00000640813.1:c.-19+41_-19+42insTGCCTGT	ENSP00000491061.1:n.-19+41_-19+42insTGCCTGT
ENST00000648026.1:c.27+41_27+42insTGCCTGT	ENSP00000498044.1:n.27+41_27+42insTGCCTGT
ENST00000649868.1:c.33+41_33+42insTGCCTGT	ENSP00000497548.1:n.33+41_33+42insTGCCTGT
ENST00000652429.1:c.33+41_33+42insTGCCTGT MANE Select	ENSP00000498786.1:n.33+41_33+42insTGCCTGT
ENST00000278715.7:c.33+41_33+42insTGCCTGT	ENSP00000278715.3:n.33+41_33+42insTGCCTGT
ENST00000442944.6:c.-102+41_-102+42insTGCCTGT	ENSP00000392041.2:n.-102+41_-102+42insTGCCTGT
ENST00000535793.5:c.33+41_33+42insTGCCTGT	ENSP00000439904.1:n.33+41_33+42insTGCCTGT
ENST00000536185.5:n.201+41_201+42insTGCCTGT
ENST00000536813.5:c.33+41_33+42insTGCCTGT	ENSP00000438726.1:n.33+41_33+42insTGCCTGT
ENST00000537841.5:c.-69_-68insTGCCTGT	ENSP00000444730.1:n.-69_-68insTGCCTGT
ENST00000542044.5:n.158+41_158+42insTGCCTGT
ENST00000542729.5:c.-69_-68insTGCCTGT	ENSP00000443058.1:n.-69_-68insTGCCTGT
ENST00000542822.5:c.74_75insTGCCTGT	ENSP00000444817.1:p.Arg26AlafsTer26
ENST00000543090.5:c.33+41_33+42insTGCCTGT	ENSP00000445429.1:n.33+41_33+42insTGCCTGT
ENST00000543821.5:n.179+41_179+42insTGCCTGT
ENST00000544387.5:c.33+41_33+42insTGCCTGT	ENSP00000438424.1:n.33+41_33+42insTGCCTGT
ENST00000545621.5:c.33+41_33+42insTGCCTGT	ENSP00000444849.1:n.33+41_33+42insTGCCTGT
ENST00000545901.5:n.186+41_186+42insTGCCTGT
ENST00000546302.5:c.33+41_33+42insTGCCTGT	ENSP00000445599.1:n.33+41_33+42insTGCCTGT
NM_000190.3:c.33+41_33+42insTGCCTGT	NP_000181.2:n.33+41_33+42insTGCCTGT
NM_001258208.1:c.33+41_33+42insTGCCTGT	NP_001245137.1:n.33+41_33+42insTGCCTGT
NM_001258209.1:c.-69_-68insTGCCTGT	NP_001245138.1:n.-69_-68insTGCCTGT
XM_005271531.1:c.-69_-68insTGCCTGT	XP_005271588.1:n.-69_-68insTGCCTGT
XM_005271532.1:c.-45_-44insTGCCTGT	XP_005271589.1:n.-45_-44insTGCCTGT
XM_005271533.2:c.33+41_33+42insTGCCTGT	XP_005271590.1:n.33+41_33+42insTGCCTGT
NM_000190.4:c.33+41_33+42insTGCCTGT MANE Select	NP_000181.2:n.33+41_33+42insTGCCTGT
XM_005271533.3:c.33+41_33+42insTGCCTGT	XP_005271590.1:n.33+41_33+42insTGCCTGT
XM_024448460.1:c.33+41_33+42insTGCCTGT	XP_024304228.1:n.33+41_33+42insTGCCTGT
NM_001258208.2:c.33+41_33+42insTGCCTGT	NP_001245137.1:n.33+41_33+42insTGCCTGT
NM_001258209.2:c.-69_-68insTGCCTGT	NP_001245138.1:n.-69_-68insTGCCTGT