Canonical Allele Identifier: CA1291522737

Gene: THSD7B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.137322384G= , CM000664.2:g.137322384G=	GRCh38
NC_000002.11:g.138079954G= , CM000664.1:g.138079954G=	GRCh37
NC_000002.10:g.137796424G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001316349.2:c.2500+46358G= MANE Select	NP_001303278.1:n.2500+46358G=
ENST00000409968.6:c.2500+46358G= MANE Select	ENSP00000387145.1:n.2500+46358G=
NM_001080427.1:c.2407+46358G=	NP_001073896.1:n.2407+46358G=
NM_001316349.1:c.2500+46358G=	NP_001303278.1:n.2500+46358G=
ENST00000272643.7:c.2500+46358G=	ENSP00000272643.4:n.2500+46358G=
ENST00000409968.5:c.2500+46358G=	ENSP00000387145.1:n.2500+46358G=
ENST00000413152.3:c.2407+46358G=	ENSP00000413841.3:n.2407+46358G=
XM_017005049.1:c.703+46358G=	XP_016860538.1:n.703+46358G=