Canonical Allele Identifier: CA1291598728

Gene: THSD7B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.137470008G= , CM000664.2:g.137470008G=	GRCh38
NC_000002.11:g.138227578G= , CM000664.1:g.138227578G=	GRCh37
NC_000002.10:g.137944048G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409968.6:c.3138+18985G= MANE Select	ENSP00000387145.1:n.3138+18985G=
ENST00000272643.7:c.3139+18984G=	ENSP00000272643.4:n.3139+18984G=
ENST00000409968.5:c.3138+18985G=	ENSP00000387145.1:n.3138+18985G=
ENST00000413152.3:c.3046+18984G=	ENSP00000413841.3:n.3046+18984G=
NM_001080427.1:c.3045+18985G=	NP_001073896.1:n.3045+18985G=
NM_001316349.1:c.3138+18985G=	NP_001303278.1:n.3138+18985G=
XM_017005049.1:c.1341+18985G=	XP_016860538.1:n.1341+18985G=
NM_001316349.2:c.3138+18985G= MANE Select	NP_001303278.1:n.3138+18985G=