Canonical Allele Identifier: CA390640714

Gene: FBLN5

Linked Data

• MyVariant Identifiers: chr14:g.92343922A>G (hg19) ; chr14:g.91877578A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91877578A>G , CM000676.2:g.91877578A>G	GRCh38
NC_000014.8:g.92343922A>G , CM000676.1:g.92343922A>G	GRCh37
NC_000014.7:g.91413675A>G	NCBI36
NG_008254.1:g.75125T>C , LRG_364:g.75125T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557088.6:c.*1060T>C	ENSP00000451002.1:n.*1060T>C
ENST00000557570.2:c.926T>C	ENSP00000450787.2:p.Ile309Thr
ENST00000706675.1:n.909T>C
ENST00000706676.1:c.1268T>C	ENSP00000516492.1:p.Ile423Thr
ENST00000706677.1:c.1094T>C	ENSP00000516493.1:p.Ile365Thr
ENST00000706678.1:n.1014T>C
ENST00000706679.1:c.926T>C	ENSP00000516494.1:p.Ile309Thr
ENST00000706680.1:c.*937T>C	ENSP00000516495.1:n.*937T>C
ENST00000706681.1:c.*833T>C	ENSP00000516496.1:n.*833T>C
ENST00000342058.9:c.1094T>C MANE Select	ENSP00000345008.4:p.Ile365Thr
ENST00000267620.14:c.1217T>C	ENSP00000267620.10:p.Ile406Thr
ENST00000342058.8:c.1094T>C	ENSP00000345008.4:p.Ile365Thr
ENST00000554121.2:n.220T>C
ENST00000556154.5:c.1109T>C	ENSP00000451982.1:p.Ile370Thr
NM_006329.3:c.1094T>C , LRG_364t1:c.1094T>C	NP_006320.2:p.Ile365Thr
XM_005267267.3:c.1145T>C	XP_005267324.1:p.Ile382Thr
XM_011536356.1:c.1145T>C	XP_011534658.1:p.Ile382Thr
XM_011536357.1:c.1094T>C	XP_011534659.1:p.Ile365Thr
XM_011536358.1:c.926T>C	XP_011534660.1:p.Ile309Thr
XM_011536357.2:c.1094T>C	XP_011534659.1:p.Ile365Thr
XM_011536358.2:c.926T>C	XP_011534660.1:p.Ile309Thr
XM_017020929.2:c.926T>C	XP_016876418.1:p.Ile309Thr
NM_001384158.1:c.1217T>C	NP_001371087.1:p.Ile406Thr
NM_001384159.1:c.1145T>C	NP_001371088.1:p.Ile382Thr
NM_001384160.1:c.1094T>C	NP_001371089.1:p.Ile365Thr
NM_001384161.1:c.926T>C	NP_001371090.1:p.Ile309Thr
NM_001384162.1:c.926T>C	NP_001371091.1:p.Ile309Thr
NM_006329.4:c.1094T>C MANE Select	NP_006320.2:p.Ile365Thr