Canonical Allele Identifier: CA390640762

Gene: FBLN5

Linked Data

• MyVariant Identifiers: chr14:g.92343934A>G (hg19) ; chr14:g.91877590A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91877590A>G , CM000676.2:g.91877590A>G	GRCh38
NC_000014.8:g.92343934A>G , CM000676.1:g.92343934A>G	GRCh37
NC_000014.7:g.91413687A>G	NCBI36
NG_008254.1:g.75113T>C , LRG_364:g.75113T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557088.6:c.*1048T>C	ENSP00000451002.1:n.*1048T>C
ENST00000557570.2:c.914T>C	ENSP00000450787.2:p.Val305Ala
ENST00000706675.1:n.897T>C
ENST00000706676.1:c.1256T>C	ENSP00000516492.1:p.Val419Ala
ENST00000706677.1:c.1082T>C	ENSP00000516493.1:p.Val361Ala
ENST00000706678.1:n.1002T>C
ENST00000706679.1:c.914T>C	ENSP00000516494.1:p.Val305Ala
ENST00000706680.1:c.*925T>C	ENSP00000516495.1:n.*925T>C
ENST00000706681.1:c.*821T>C	ENSP00000516496.1:n.*821T>C
ENST00000342058.9:c.1082T>C MANE Select	ENSP00000345008.4:p.Val361Ala
ENST00000267620.14:c.1205T>C	ENSP00000267620.10:p.Val402Ala
ENST00000342058.8:c.1082T>C	ENSP00000345008.4:p.Val361Ala
ENST00000554121.2:n.208T>C
ENST00000556154.5:c.1097T>C	ENSP00000451982.1:p.Val366Ala
NM_006329.3:c.1082T>C , LRG_364t1:c.1082T>C	NP_006320.2:p.Val361Ala
XM_005267267.3:c.1133T>C	XP_005267324.1:p.Val378Ala
XM_011536356.1:c.1133T>C	XP_011534658.1:p.Val378Ala
XM_011536357.1:c.1082T>C	XP_011534659.1:p.Val361Ala
XM_011536358.1:c.914T>C	XP_011534660.1:p.Val305Ala
XM_011536357.2:c.1082T>C	XP_011534659.1:p.Val361Ala
XM_011536358.2:c.914T>C	XP_011534660.1:p.Val305Ala
XM_017020929.2:c.914T>C	XP_016876418.1:p.Val305Ala
NM_001384158.1:c.1205T>C	NP_001371087.1:p.Val402Ala
NM_001384159.1:c.1133T>C	NP_001371088.1:p.Val378Ala
NM_001384160.1:c.1082T>C	NP_001371089.1:p.Val361Ala
NM_001384161.1:c.914T>C	NP_001371090.1:p.Val305Ala
NM_001384162.1:c.914T>C	NP_001371091.1:p.Val305Ala
NM_006329.4:c.1082T>C MANE Select	NP_006320.2:p.Val361Ala