Canonical Allele Identifier: CA2602697556

Gene: FLNA

Linked Data

• gnomAD v3: X-154371481-C-CCG
• gnomAD v4: X-154371481-C-CCG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371481_154371482insCG , CM000685.2:g.154371481_154371482insCG	GRCh38
NC_000023.10:g.153599849_153599850insCG , CM000685.1:g.153599849_153599850insCG	GRCh37
NC_000023.9:g.153253043_153253044insCG	NCBI36
NG_008677.1:g.2054_2055insCG , LRG_745:g.2054_2055insCG
NG_011506.1:g.8157_8158insCG
NG_011506.2:g.8157_8158insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369850.10:c.-116-121_-116-120insCG MANE Select	ENSP00000358866.3:n.-116-121_-116-120insCG
ENST00000369850.7:c.-116-121_-116-120insCG	ENSP00000358866.3:n.-116-121_-116-120insCG
ENST00000422373.5:c.-116-121_-116-120insCG	ENSP00000416926.1:n.-116-121_-116-120insCG
ENST00000610817.4:c.-197-121_-197-120insCG	ENSP00000480593.1:n.-197-121_-197-120insCG
NM_001110556.1:c.-116-121_-116-120insCG	NP_001104026.1:n.-116-121_-116-120insCG
NM_001456.3:c.-116-121_-116-120insCG	NP_001447.2:n.-116-121_-116-120insCG
XM_011531127.1:c.-116-121_-116-120insCG	XP_011529429.1:n.-116-121_-116-120insCG
XM_011531128.1:c.-116-121_-116-120insCG	XP_011529430.1:n.-116-121_-116-120insCG
XM_011531129.1:c.-116-121_-116-120insCG	XP_011529431.1:n.-116-121_-116-120insCG
XM_011531130.1:c.-116-121_-116-120insCG	XP_011529432.1:n.-116-121_-116-120insCG
XM_011531131.1:c.-116-121_-116-120insCG	XP_011529433.1:n.-116-121_-116-120insCG
NM_001110556.2:c.-116-121_-116-120insCG MANE Select	NP_001104026.1:n.-116-121_-116-120insCG
NM_001456.4:c.-116-121_-116-120insCG	NP_001447.2:n.-116-121_-116-120insCG