Canonical Allele Identifier: CA265591807

Gene: FBLN5

Linked Data

• dbSNP Id: rs967284914
• gnomAD v4: 14-91870447-C-A
• MyVariant Identifiers: chr14:g.92336791C>A (hg19) ; chr14:g.91870447C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91870447C>A , CM000676.2:g.91870447C>A	GRCh38
NC_000014.8:g.92336791C>A , CM000676.1:g.92336791C>A	GRCh37
NC_000014.7:g.91406544C>A	NCBI36
NG_008254.1:g.82256G>T , LRG_364:g.82256G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557088.6:c.*1152-62G>T	ENSP00000451002.1:n.*1152-62G>T
ENST00000557570.2:c.1018-62G>T	ENSP00000450787.2:n.1018-62G>T
ENST00000706675.1:n.1001-62G>T
ENST00000706676.1:c.1360-62G>T	ENSP00000516492.1:n.1360-62G>T
ENST00000706677.1:c.1365-62G>T	ENSP00000516493.1:n.1365-62G>T
ENST00000706678.1:n.1106-62G>T
ENST00000706679.1:c.1018-62G>T	ENSP00000516494.1:n.1018-62G>T
ENST00000706680.1:c.*1029-62G>T	ENSP00000516495.1:n.*1029-62G>T
ENST00000706681.1:c.*925-62G>T	ENSP00000516496.1:n.*925-62G>T
ENST00000342058.9:c.1186-62G>T MANE Select	ENSP00000345008.4:n.1186-62G>T
ENST00000267620.14:c.1309-62G>T	ENSP00000267620.10:n.1309-62G>T
ENST00000342058.8:c.1186-62G>T	ENSP00000345008.4:n.1186-62G>T
ENST00000554121.2:n.312-62G>T
ENST00000556154.5:c.1201-62G>T	ENSP00000451982.1:n.1201-62G>T
ENST00000556961.1:n.1321-62G>T
NM_006329.3:c.1186-62G>T , LRG_364t1:c.1186-62G>T	NP_006320.2:n.1186-62G>T
XM_005267267.3:c.1237-62G>T	XP_005267324.1:n.1237-62G>T
XM_011536356.1:c.1416-62G>T	XP_011534658.1:n.1416-62G>T
XM_011536357.1:c.1365-62G>T	XP_011534659.1:n.1365-62G>T
XM_011536358.1:c.1197-62G>T	XP_011534660.1:n.1197-62G>T
XM_011536357.2:c.1365-62G>T	XP_011534659.1:n.1365-62G>T
XM_011536358.2:c.1197-62G>T	XP_011534660.1:n.1197-62G>T
XM_017020929.2:c.1018-62G>T	XP_016876418.1:n.1018-62G>T
NM_001384158.1:c.1309-62G>T	NP_001371087.1:n.1309-62G>T
NM_001384159.1:c.1237-62G>T	NP_001371088.1:n.1237-62G>T
NM_001384160.1:c.1365-62G>T	NP_001371089.1:n.1365-62G>T
NM_001384161.1:c.1197-62G>T	NP_001371090.1:n.1197-62G>T
NM_001384162.1:c.1018-62G>T	NP_001371091.1:n.1018-62G>T
NM_006329.4:c.1186-62G>T MANE Select	NP_006320.2:n.1186-62G>T