Canonical Allele Identifier: CA669665314

Gene: ACTA2 FAS

Linked Data

• dbSNP Id: rs1260188723
• gnomAD v3: 10-88990164-G-GC
• gnomAD v4: 10-88990164-G-GC
• MyVariant Identifiers: chr10:g.90749921_90749922insC (hg19) ; chr10:g.88990164_88990165insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.88990165dup , CM000672.2:g.88990165dup	GRCh38
NC_000010.10:g.90749922dup , CM000672.1:g.90749922dup	GRCh37
NC_000010.9:g.90739902dup	NCBI36
NG_009089.2:g.4635dup , LRG_134:g.4635dup
NG_011541.1:g.6226dup , LRG_781:g.6226dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000415557.2:c.-24+774dup (ACTA2)	ENSP00000396730.2:n.-24+774dup
ENST00000458159.6:c.-24+857dup (ACTA2)	ENSP00000398239.2:n.-24+857dup
ENST00000696723.1:n.3663+586dup (FAS)
ENST00000696992.1:n.1147+586dup (FAS)
ENST00000688239.1:n.372-41dup (FAS)
ENST00000690268.1:c.111+586dup (FAS)	ENSP00000509810.1:n.111+586dup
ENST00000415557.1:c.-24+774dup (ACTA2)	ENSP00000396730.1:n.-24+774dup
ENST00000458159.5:c.-24+857dup (ACTA2)	ENSP00000398239.1:n.-24+857dup
ENST00000458208.5:c.-24+774dup (ACTA2)	ENSP00000402373.1:n.-24+774dup
NM_001141945.1:c.-24+774dup , LRG_781t2:c.-24+774dup (ACTA2)	NP_001135417.1:n.-24+774dup
XM_006717819.2:c.111+586dup (FAS)	XP_006717882.1:n.111+586dup
XM_011539764.1:c.192+586dup (FAS)	XP_011538066.1:n.192+586dup
XM_011539765.1:c.192+586dup (FAS)	XP_011538067.1:n.192+586dup
XM_011539766.1:c.111+586dup (FAS)	XP_011538068.1:n.111+586dup
XM_011540016.1:c.-24+857dup (ACTA2)	XP_011538318.1:n.-24+857dup
XR_945732.1:n.207+586dup (FAS)
XR_945733.1:n.207+586dup (FAS)
NM_001141945.2:c.-24+774dup (ACTA2)	NP_001135417.1:n.-24+774dup
NM_001320855.1:c.-24+857dup (ACTA2)	NP_001307784.1:n.-24+857dup
XM_006717819.3:c.111+586dup (FAS)	XP_006717882.1:n.111+586dup
XM_011539764.2:c.192+586dup (FAS)	XP_011538066.1:n.192+586dup
XM_011539765.2:c.192+586dup (FAS)	XP_011538067.1:n.192+586dup
XM_011539766.2:c.111+586dup (FAS)	XP_011538068.1:n.111+586dup
XR_945732.3:n.207+586dup (FAS)
XR_945733.2:n.207+586dup (FAS)