Canonical Allele Identifier: CA2695113780

Gene: FLNA

Linked Data

• gnomAD v4: X-154371262-CCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371263_154371264del , CM000685.2:g.154371263_154371264del	GRCh38
NC_000023.10:g.153599631_153599632del , CM000685.1:g.153599631_153599632del	GRCh37
NC_000023.9:g.153252825_153252826del	NCBI36
NG_008677.1:g.1836_1837del , LRG_745:g.1836_1837del
NG_011506.1:g.8375_8376del
NG_011506.2:g.8375_8376del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.-19_-18del	ENSP00000353467.4:n.-19_-18del
ENST00000369850.10:c.-19_-18del MANE Select	ENSP00000358866.3:n.-19_-18del
ENST00000422373.6:c.-19_-18del	ENSP00000416926.2:n.-19_-18del
ENST00000344736.8:c.-19_-18del	ENSP00000358863.3:n.-19_-18del
ENST00000360319.8:c.-19_-18del	ENSP00000353467.4:n.-19_-18del
ENST00000369850.7:c.-19_-18del	ENSP00000358866.3:n.-19_-18del
ENST00000422373.5:c.-19_-18del	ENSP00000416926.1:n.-19_-18del
ENST00000610817.4:c.-100_-99del	ENSP00000480593.1:n.-100_-99del
NM_001110556.1:c.-19_-18del	NP_001104026.1:n.-19_-18del
NM_001456.3:c.-19_-18del	NP_001447.2:n.-19_-18del
XM_011531127.1:c.-19_-18del	XP_011529429.1:n.-19_-18del
XM_011531128.1:c.-19_-18del	XP_011529430.1:n.-19_-18del
XM_011531129.1:c.-19_-18del	XP_011529431.1:n.-19_-18del
XM_011531130.1:c.-19_-18del	XP_011529432.1:n.-19_-18del
XM_011531131.1:c.-19_-18del	XP_011529433.1:n.-19_-18del
NM_001110556.2:c.-19_-18del MANE Select	NP_001104026.1:n.-19_-18del
NM_001456.4:c.-19_-18del	NP_001447.2:n.-19_-18del