Canonical Allele Identifier: CA777156

Gene: FHL3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.37998998C>T , CM000663.2:g.37998998C>T	GRCh38
NC_000001.10:g.38464670C>T , CM000663.1:g.38464670C>T	GRCh37
NC_000001.9:g.38237257C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373016.4:c.307G>A MANE Select	ENSP00000362107.3:p.Ala103Thr
ENST00000373016.3:c.307G>A	ENSP00000362107.3:p.Ala103Thr
ENST00000475084.5:n.297G>A
ENST00000477194.5:n.495G>A
ENST00000483132.1:n.327G>A
ENST00000485803.5:n.297G>A
NM_001243878.1:c.-18G>A	NP_001230807.1:n.-18G>A
NM_004468.4:c.307G>A	NP_004459.2:p.Ala103Thr
XM_017000675.1:c.78G>A	XP_016856164.1:p.Pro26=
XM_024454099.1:c.307G>A	XP_024309867.1:p.Ala103Thr
XM_024454100.1:c.307G>A	XP_024309868.1:p.Ala103Thr
XM_024454101.1:c.307G>A	XP_024309869.1:p.Ala103Thr
NM_004468.5:c.307G>A MANE Select	NP_004459.2:p.Ala103Thr
NM_001243878.2:c.-18G>A	NP_001230807.1:n.-18G>A