Canonical Allele Identifier: CA873335132

Gene: FLNA

Linked Data

• dbSNP Id: rs1253116708
• gnomAD v3: X-154350601-CTGCCCCAGGCCTG-C
• gnomAD v4: X-154350601-CTGCCCCAGGCCTG-C
• MyVariant Identifiers: chrX:g.154350602_154350614del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350605_154350617del , CM000685.2:g.154350605_154350617del	GRCh38
NC_000023.10:g.153578973_153578985del , CM000685.1:g.153578973_153578985del	GRCh37
NC_000023.9:g.153232167_153232179del	NCBI36
NG_011506.1:g.29025_29037del
NG_011506.2:g.29025_29037del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7132+295_7132+307del	ENSP00000353467.4:n.7132+295_7132+307del
ENST00000369850.10:c.7156+295_7156+307del MANE Select	ENSP00000358866.3:n.7156+295_7156+307del
ENST00000369856.8:c.7075+295_7075+307del	ENSP00000358872.4:n.7075+295_7075+307del
ENST00000422373.6:c.3937+295_3937+307del	ENSP00000416926.2:n.3937+295_3937+307del
ENST00000610817.5:c.7213+295_7213+307del	ENSP00000480593.2:n.7213+295_7213+307del
ENST00000673639.2:c.280-1924_280-1912del
ENST00000676696.1:c.7435+295_7435+307del	ENSP00000503392.1:n.7435+295_7435+307del
ENST00000678304.1:n.2874+295_2874+307del
ENST00000344736.8:c.7036+295_7036+307del	ENSP00000358863.3:n.7036+295_7036+307del
ENST00000360319.8:c.7132+295_7132+307del	ENSP00000353467.4:n.7132+295_7132+307del
ENST00000369850.7:c.7156+295_7156+307del	ENSP00000358866.3:n.7156+295_7156+307del
ENST00000369856.7:c.7075+295_7075+307del	ENSP00000358872.4:n.7075+295_7075+307del
ENST00000420627.5:c.7112+295_7112+307del	ENSP00000408921.1:n.7112+295_7112+307del
ENST00000422373.5:c.7132+295_7132+307del	ENSP00000416926.1:n.7132+295_7132+307del
ENST00000490936.5:n.3979_3991del
ENST00000498411.1:n.68-1784_68-1772del
ENST00000498491.5:n.197+295_197+307del
ENST00000610817.4:c.6160+295_6160+307del	ENSP00000480593.1:n.6160+295_6160+307del
NM_001110556.1:c.7156+295_7156+307del	NP_001104026.1:n.7156+295_7156+307del
NM_001456.3:c.7132+295_7132+307del	NP_001447.2:n.7132+295_7132+307del
XM_011531127.1:c.7060+295_7060+307del	XP_011529429.1:n.7060+295_7060+307del
XM_011531128.1:c.7036+295_7036+307del	XP_011529430.1:n.7036+295_7036+307del
XM_011531129.1:c.6982+295_6982+307del	XP_011529431.1:n.6982+295_6982+307del
XM_011531130.1:c.6958+295_6958+307del	XP_011529432.1:n.6958+295_6958+307del
XM_011531131.1:c.6955+295_6955+307del	XP_011529433.1:n.6955+295_6955+307del
NM_001110556.2:c.7156+295_7156+307del MANE Select	NP_001104026.1:n.7156+295_7156+307del
NM_001456.4:c.7132+295_7132+307del	NP_001447.2:n.7132+295_7132+307del