Canonical Allele Identifier: CA1926617950

Gene: ACTA2 FAS

Linked Data

• dbSNP Id: rs1847082585

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.88990275C>G , CM000672.2:g.88990275C>G	GRCh38
NC_000010.10:g.90750032C>G , CM000672.1:g.90750032C>G	GRCh37
NC_000010.9:g.90740012C>G	NCBI36
NG_009089.2:g.4745C>G , LRG_134:g.4745C>G
NG_011541.1:g.6116G>C , LRG_781:g.6116G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000415557.2:c.-24+664G>C (ACTA2)	ENSP00000396730.2:n.-24+664G>C
ENST00000458159.6:c.-24+747G>C (ACTA2)	ENSP00000398239.2:n.-24+747G>C
ENST00000696723.1:n.3663+696C>G (FAS)
ENST00000696992.1:n.1147+696C>G (FAS)
ENST00000688239.1:n.441C>G (FAS)
ENST00000690268.1:c.111+696C>G (FAS)	ENSP00000509810.1:n.111+696C>G
ENST00000415557.1:c.-24+664G>C (ACTA2)	ENSP00000396730.1:n.-24+664G>C
ENST00000458159.5:c.-24+747G>C (ACTA2)	ENSP00000398239.1:n.-24+747G>C
ENST00000458208.5:c.-24+664G>C (ACTA2)	ENSP00000402373.1:n.-24+664G>C
NM_001141945.1:c.-24+664G>C , LRG_781t2:c.-24+664G>C (ACTA2)	NP_001135417.1:n.-24+664G>C
XM_006717819.2:c.111+696C>G (FAS)	XP_006717882.1:n.111+696C>G
XM_011539764.1:c.192+696C>G (FAS)	XP_011538066.1:n.192+696C>G
XM_011539765.1:c.192+696C>G (FAS)	XP_011538067.1:n.192+696C>G
XM_011539766.1:c.111+696C>G (FAS)	XP_011538068.1:n.111+696C>G
XM_011540016.1:c.-24+747G>C (ACTA2)	XP_011538318.1:n.-24+747G>C
XR_945732.1:n.207+696C>G (FAS)
XR_945733.1:n.207+696C>G (FAS)
NM_001141945.2:c.-24+664G>C (ACTA2)	NP_001135417.1:n.-24+664G>C
NM_001320855.1:c.-24+747G>C (ACTA2)	NP_001307784.1:n.-24+747G>C
XM_006717819.3:c.111+696C>G (FAS)	XP_006717882.1:n.111+696C>G
XM_011539764.2:c.192+696C>G (FAS)	XP_011538066.1:n.192+696C>G
XM_011539765.2:c.192+696C>G (FAS)	XP_011538067.1:n.192+696C>G
XM_011539766.2:c.111+696C>G (FAS)	XP_011538068.1:n.111+696C>G
XR_945732.3:n.207+696C>G (FAS)
XR_945733.2:n.207+696C>G (FAS)