Canonical Allele Identifier: CA2081916854

Gene: HMGB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.30459049_30459052delinsTATA , CM000675.2:g.30459049_30459052delinsTATA	GRCh38
NC_000013.10:g.31033186_31033189delinsTATA , CM000675.1:g.31033186_31033189delinsTATA	GRCh37
NC_000013.9:g.29931186_29931189delinsTATA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341423.10:c.*2305_*2308delinsTATA MANE Select	ENSP00000345347.5:n.*2305_*2308delinsTATA
ENST00000341423.9:c.*2305_*2308delinsTATA	ENSP00000345347.5:n.*2305_*2308delinsTATA
ENST00000405805.5:c.*2305_*2308delinsTATA	ENSP00000384678.1:n.*2305_*2308delinsTATA
NM_001313892.1:c.*2305_*2308delinsTATA	NP_001300821.1:n.*2305_*2308delinsTATA
NM_001313893.1:c.*2305_*2308delinsTATA	NP_001300822.1:n.*2305_*2308delinsTATA
NM_002128.4:c.*2305_*2308delinsTATA	NP_002119.1:n.*2305_*2308delinsTATA
NM_002128.5:c.*2305_*2308delinsTATA	NP_002119.1:n.*2305_*2308delinsTATA
NM_001363661.1:c.*2526_*2529delinsTATA	NP_001350590.1:n.*2526_*2529delinsTATA
NM_002128.6:c.*2305_*2308delinsTATA	NP_002119.1:n.*2305_*2308delinsTATA
NM_002128.7:c.*2305_*2308delinsTATA MANE Select	NP_002119.1:n.*2305_*2308delinsTATA
NM_001370339.1:c.*2631_*2634delinsTATA	NP_001357268.1:n.*2631_*2634delinsTATA
NM_001370340.1:c.*2305_*2308delinsTATA	NP_001357269.1:n.*2305_*2308delinsTATA
NM_001370341.1:c.*2305_*2308delinsTATA	NP_001357270.1:n.*2305_*2308delinsTATA
NM_001313892.2:c.*2305_*2308delinsTATA	NP_001300821.1:n.*2305_*2308delinsTATA
NM_001363661.2:c.*2526_*2529delinsTATA	NP_001350590.1:n.*2526_*2529delinsTATA