Canonical Allele Identifier: CA1508312359

Gene: FSTL5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.161681057G= , CM000666.2:g.161681057G=	GRCh38
NC_000004.11:g.162602209G= , CM000666.1:g.162602209G=	GRCh37
NC_000004.10:g.162821659G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_020116.5:c.728-24563C= MANE Select	NP_064501.2:n.728-24563C=
ENST00000306100.10:c.728-24563C= MANE Select	ENSP00000305334.4:n.728-24563C=
NM_001128427.2:c.725-24563C=	NP_001121899.1:n.725-24563C=
NM_001128427.3:c.725-24563C=	NP_001121899.1:n.725-24563C=
NM_001128428.2:c.725-24563C=	NP_001121900.1:n.725-24563C=
NM_001128428.3:c.725-24563C=	NP_001121900.1:n.725-24563C=
NM_020116.4:c.728-24563C=	NP_064501.2:n.728-24563C=
ENST00000306100.9:c.728-24563C=	ENSP00000305334.4:n.728-24563C=
ENST00000379164.8:c.725-24563C=	ENSP00000368462.4:n.725-24563C=
ENST00000427802.2:c.725-24563C=	ENSP00000389270.2:n.725-24563C=
XM_011532126.1:c.728-24563C=	XP_011530428.1:n.728-24563C=