Canonical Allele Identifier: CA211320353

Gene: ACTA2 FAS

Linked Data

• dbSNP Id: rs930485104
• gnomAD v3: 10-88989514-C-T
• gnomAD v4: 10-88989514-C-T
• MyVariant Identifiers: chr10:g.90749271C>T (hg19) ; chr10:g.88989514C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.88989514C>T , CM000672.2:g.88989514C>T	GRCh38
NC_000010.10:g.90749271C>T , CM000672.1:g.90749271C>T	GRCh37
NC_000010.9:g.90739251C>T	NCBI36
NG_009089.2:g.3984C>T , LRG_134:g.3984C>T
NG_011541.1:g.6877G>A , LRG_781:g.6877G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000415557.2:c.-24+1425G>A (ACTA2)	ENSP00000396730.2:n.-24+1425G>A
ENST00000458159.6:c.-24+1508G>A (ACTA2)	ENSP00000398239.2:n.-24+1508G>A
ENST00000696723.1:n.3598C>T (FAS)
ENST00000696992.1:n.1082C>T (FAS)
ENST00000688239.1:n.306C>T (FAS)
ENST00000690268.1:c.46C>T (FAS)	ENSP00000509810.1:p.His16Tyr
ENST00000415557.1:c.-24+1425G>A (ACTA2)	ENSP00000396730.1:n.-24+1425G>A
ENST00000458159.5:c.-24+1508G>A (ACTA2)	ENSP00000398239.1:n.-24+1508G>A
ENST00000458208.5:c.-24+1425G>A (ACTA2)	ENSP00000402373.1:n.-24+1425G>A
NM_001141945.1:c.-24+1425G>A , LRG_781t2:c.-24+1425G>A (ACTA2)	NP_001135417.1:n.-24+1425G>A
XM_006717819.2:c.46C>T (FAS)	XP_006717882.1:p.His16Tyr
XM_011539764.1:c.127C>T (FAS)	XP_011538066.1:p.His43Tyr
XM_011539765.1:c.127C>T (FAS)	XP_011538067.1:p.His43Tyr
XM_011539766.1:c.46C>T (FAS)	XP_011538068.1:p.His16Tyr
XM_011540016.1:c.-24+1508G>A (ACTA2)	XP_011538318.1:n.-24+1508G>A
XR_945732.1:n.142C>T (FAS)
XR_945733.1:n.142C>T (FAS)
NM_001141945.2:c.-24+1425G>A (ACTA2)	NP_001135417.1:n.-24+1425G>A
NM_001320855.1:c.-24+1508G>A (ACTA2)	NP_001307784.1:n.-24+1508G>A
XM_006717819.3:c.46C>T (FAS)	XP_006717882.1:p.His16Tyr
XM_011539764.2:c.127C>T (FAS)	XP_011538066.1:p.His43Tyr
XM_011539765.2:c.127C>T (FAS)	XP_011538067.1:p.His43Tyr
XM_011539766.2:c.46C>T (FAS)	XP_011538068.1:p.His16Tyr
XR_945732.3:n.142C>T (FAS)
XR_945733.2:n.142C>T (FAS)