Canonical Allele Identifier: CA2518454577
Gene: THSD7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.137469849_137469850insCGCTTCACAAACGAGGAACTACTCGTTGGCTACATACAGCATAAAACAGGGAAGGGACATGATGATTTCTCTTCGTTACAACCGCAATACTTAAAACCAGGAAAAGGTGTTCGTTGGCATAAACCAG , CM000664.2:g.137469849_137469850insCGCTTCACAAACGAGGAACTACTCGTTGGCTACATACAGCATAAAACAGGGAAGGGACATGATGATTTCTCTTCGTTACAACCGCAATACTTAAAACCAGGAAAAGGTGTTCGTTGGCATAAACCAG GRCh38
NC_000002.11:g.138227419_138227420insCGCTTCACAAACGAGGAACTACTCGTTGGCTACATACAGCATAAAACAGGGAAGGGACATGATGATTTCTCTTCGTTACAACCGCAATACTTAAAACCAGGAAAAGGTGTTCGTTGGCATAAACCAG , CM000664.1:g.138227419_138227420insCGCTTCACAAACGAGGAACTACTCGTTGGCTACATACAGCATAAAACAGGGAAGGGACATGATGATTTCTCTTCGTTACAACCGCAATACTTAAAACCAGGAAAAGGTGTTCGTTGGCATAAACCAG GRCh37
NC_000002.10:g.137943889_137943890insCGCTTCACAAACGAGGAACTACTCGTTGGCTACATACAGCATAAAACAGGGAAGGGACATGATGATTTCTCTTCGTTACAACCGCAATACTTAAAACCAGGAAAAGGTGTTCGTTGGCATAAACCAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000409968.6:c.3138+18826_3138+18827insCGCTTCACAAACGAGGAACTACTCGTTGGCTACATACAGCATAAAACAGGGAAGGGACATGATGATTTCTCTTCGTTACAACCGCAATACTTAAAACCAGGAAAAGGTGTTCGTTGGCATAAACCAG MANE Select ENSP00000387145.1:n.3138+18826_3138+18827insCGCTTCACAAACGAGGA...
ENST00000272643.7:c.3139+18825_3139+18826insCGCTTCACAAACGAGGAACTACTCGTTGGCTACATACAGCATAAAACAGGGAAGGGACATGATGATTTCTCTTCGTTACAACCGCAATACTTAAAACCAGGAAAAGGTGTTCGTTGGCATAAACCAG ENSP00000272643.4:n.3139+18825_3139+18826insCGCTTCACAAACGAGGA...
ENST00000409968.5:c.3138+18826_3138+18827insCGCTTCACAAACGAGGAACTACTCGTTGGCTACATACAGCATAAAACAGGGAAGGGACATGATGATTTCTCTTCGTTACAACCGCAATACTTAAAACCAGGAAAAGGTGTTCGTTGGCATAAACCAG ENSP00000387145.1:n.3138+18826_3138+18827insCGCTTCACAAACGAGGA...
ENST00000413152.3:c.3046+18825_3046+18826insCGCTTCACAAACGAGGAACTACTCGTTGGCTACATACAGCATAAAACAGGGAAGGGACATGATGATTTCTCTTCGTTACAACCGCAATACTTAAAACCAGGAAAAGGTGTTCGTTGGCATAAACCAG ENSP00000413841.3:n.3046+18825_3046+18826insCGCTTCACAAACGAGGA...
NM_001080427.1:c.3045+18826_3045+18827insCGCTTCACAAACGAGGAACTACTCGTTGGCTACATACAGCATAAAACAGGGAAGGGACATGATGATTTCTCTTCGTTACAACCGCAATACTTAAAACCAGGAAAAGGTGTTCGTTGGCATAAACCAG NP_001073896.1:n.3045+18826_3045+18827insCGCTTCACAAACGAGGAACT...
NM_001316349.1:c.3138+18826_3138+18827insCGCTTCACAAACGAGGAACTACTCGTTGGCTACATACAGCATAAAACAGGGAAGGGACATGATGATTTCTCTTCGTTACAACCGCAATACTTAAAACCAGGAAAAGGTGTTCGTTGGCATAAACCAG NP_001303278.1:n.3138+18826_3138+18827insCGCTTCACAAACGAGGAACT...
XM_017005049.1:c.1341+18826_1341+18827insCGCTTCACAAACGAGGAACTACTCGTTGGCTACATACAGCATAAAACAGGGAAGGGACATGATGATTTCTCTTCGTTACAACCGCAATACTTAAAACCAGGAAAAGGTGTTCGTTGGCATAAACCAG XP_016860538.1:n.1341+18826_1341+18827insCGCTTCACAAACGAGGAACT...
NM_001316349.2:c.3138+18826_3138+18827insCGCTTCACAAACGAGGAACTACTCGTTGGCTACATACAGCATAAAACAGGGAAGGGACATGATGATTTCTCTTCGTTACAACCGCAATACTTAAAACCAGGAAAAGGTGTTCGTTGGCATAAACCAG MANE Select NP_001303278.1:n.3138+18826_3138+18827insCGCTTCACAAACGAGGAACT...