Canonical Allele Identifier: CA1291431462

Gene: THSD7B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.137118228_137118229delinsAG , CM000664.2:g.137118228_137118229delinsAG	GRCh38
NC_000002.11:g.137875798_137875799delinsAG , CM000664.1:g.137875798_137875799delinsAG	GRCh37
NC_000002.10:g.137592268_137592269delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409968.6:c.1369+2935_1369+2936delinsAG MANE Select	ENSP00000387145.1:n.1369+2935_1369+2936delinsAG
ENST00000272643.7:c.1369+2935_1369+2936delinsAG	ENSP00000272643.4:n.1369+2935_1369+2936delinsAG
ENST00000409968.5:c.1369+2935_1369+2936delinsAG	ENSP00000387145.1:n.1369+2935_1369+2936delinsAG
ENST00000413152.3:c.1276+2935_1276+2936delinsAG	ENSP00000413841.3:n.1276+2935_1276+2936delinsAG
NM_001080427.1:c.1276+2935_1276+2936delinsAG	NP_001073896.1:n.1276+2935_1276+2936delinsAG
NM_001316349.1:c.1369+2935_1369+2936delinsAG	NP_001303278.1:n.1369+2935_1369+2936delinsAG
NM_001316349.2:c.1369+2935_1369+2936delinsAG MANE Select	NP_001303278.1:n.1369+2935_1369+2936delinsAG