Canonical Allele Identifier: CA1583553897

Gene: FSTL4

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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