Canonical Allele Identifier: CA1926617637

Gene: ACTA2 FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.88990028A= , CM000672.2:g.88990028A=	GRCh38
NC_000010.10:g.90749785A= , CM000672.1:g.90749785A=	GRCh37
NC_000010.9:g.90739765A=	NCBI36
NG_009089.2:g.4498A= , LRG_134:g.4498A=
NG_011541.1:g.6363T= , LRG_781:g.6363T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415557.2:c.-24+911T= (ACTA2)	ENSP00000396730.2:n.-24+911T=
ENST00000458159.6:c.-24+994T= (ACTA2)	ENSP00000398239.2:n.-24+994T=
ENST00000696723.1:n.3663+449A= (FAS)
ENST00000696992.1:n.1147+449A= (FAS)
ENST00000688239.1:n.372-178A= (FAS)
ENST00000690268.1:c.111+449A= (FAS)	ENSP00000509810.1:n.111+449A=
ENST00000415557.1:c.-24+911T= (ACTA2)	ENSP00000396730.1:n.-24+911T=
ENST00000458159.5:c.-24+994T= (ACTA2)	ENSP00000398239.1:n.-24+994T=
ENST00000458208.5:c.-24+911T= (ACTA2)	ENSP00000402373.1:n.-24+911T=
NM_001141945.1:c.-24+911T= , LRG_781t2:c.-24+911T= (ACTA2)	NP_001135417.1:n.-24+911T=
XM_006717819.2:c.111+449A= (FAS)	XP_006717882.1:n.111+449A=
XM_011539764.1:c.192+449A= (FAS)	XP_011538066.1:n.192+449A=
XM_011539765.1:c.192+449A= (FAS)	XP_011538067.1:n.192+449A=
XM_011539766.1:c.111+449A= (FAS)	XP_011538068.1:n.111+449A=
XM_011540016.1:c.-24+994T= (ACTA2)	XP_011538318.1:n.-24+994T=
XR_945732.1:n.207+449A= (FAS)
XR_945733.1:n.207+449A= (FAS)
NM_001141945.2:c.-24+911T= (ACTA2)	NP_001135417.1:n.-24+911T=
NM_001320855.1:c.-24+994T= (ACTA2)	NP_001307784.1:n.-24+994T=
XM_006717819.3:c.111+449A= (FAS)	XP_006717882.1:n.111+449A=
XM_011539764.2:c.192+449A= (FAS)	XP_011538066.1:n.192+449A=
XM_011539765.2:c.192+449A= (FAS)	XP_011538067.1:n.192+449A=
XM_011539766.2:c.111+449A= (FAS)	XP_011538068.1:n.111+449A=
XR_945732.3:n.207+449A= (FAS)
XR_945733.2:n.207+449A= (FAS)