Canonical Allele Identifier: CA381310167

Gene: CFL1 SNX32

Linked Data

• MyVariant Identifiers: chr11:g.65623472T>C (hg19) ; chr11:g.65856001T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65856001T>C , CM000673.2:g.65856001T>C	GRCh38
NC_000011.9:g.65623472T>C , CM000673.1:g.65623472T>C	GRCh37
NC_000011.8:g.65380048T>C	NCBI36
NG_053116.1:g.940T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308162.10:c.245A>G (CFL1) MANE Select	ENSP00000309629.5:p.Tyr82Cys
ENST00000308162.9:c.245A>G (CFL1)	ENSP00000309629.5:p.Tyr82Cys
ENST00000524553.5:c.194A>G (CFL1)	ENSP00000432226.1:p.Tyr65Cys
ENST00000525451.6:c.245A>G (CFL1)	ENSP00000432660.1:p.Tyr82Cys
ENST00000526975.1:c.245A>G (CFL1)	ENSP00000432153.1:p.Tyr82Cys
ENST00000527344.5:c.194A>G (CFL1)	ENSP00000432155.1:p.Tyr65Cys
ENST00000527752.1:n.61+2096A>G (CFL1)
ENST00000530101.5:n.1649-128T>C (SNX32)
ENST00000530413.1:c.194A>G (CFL1)	ENSP00000436899.1:p.Tyr65Cys
ENST00000530945.1:n.340A>G (CFL1)
ENST00000531407.5:c.194A>G (CFL1)	ENSP00000433910.1:p.Tyr65Cys
ENST00000531413.5:c.194A>G (CFL1)	ENSP00000433131.1:p.Tyr65Cys
ENST00000532134.5:c.245A>G (CFL1)	ENSP00000436431.1:p.Tyr82Cys
ENST00000534769.5:c.359A>G (CFL1)	ENSP00000431696.1:p.Tyr120Cys
ENST00000534784.1:c.194A>G (CFL1)	ENSP00000433308.1:p.Tyr65Cys
NM_005507.2:c.245A>G (CFL1)	NP_005498.1:p.Tyr82Cys
NM_005507.3:c.245A>G (CFL1) MANE Select	NP_005498.1:p.Tyr82Cys