Canonical Allele Identifier: CA1583553896

Gene: FSTL4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.133293192G= , CM000667.2:g.133293192G=	GRCh38
NC_000005.9:g.132628884G= , CM000667.1:g.132628884G=	GRCh37
NC_000005.8:g.132656783G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265342.12:c.727+19462C= MANE Select	ENSP00000265342.7:n.727+19462C=
ENST00000265342.11:c.727+19462C=	ENSP00000265342.7:n.727+19462C=
ENST00000621681.4:c.232-43627C=	ENSP00000484273.1:n.232-43627C=
NM_015082.1:c.727+19462C=	NP_055897.1:n.727+19462C=
XM_011543283.1:c.727+19462C=	XP_011541585.1:n.727+19462C=
XM_011543284.1:c.727+19462C=	XP_011541586.1:n.727+19462C=
XM_011543285.1:c.610+19462C=	XP_011541587.1:n.610+19462C=
XM_011543286.1:c.304+19462C=	XP_011541588.1:n.304+19462C=
XM_011543284.2:c.727+19462C=	XP_011541586.1:n.727+19462C=
XM_011543286.3:c.304+19462C=	XP_011541588.1:n.304+19462C=
NM_015082.2:c.727+19462C= MANE Select	NP_055897.1:n.727+19462C=