Canonical Allele Identifier: CA115775
Gene: FRAS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2813
ClinVar RCV Id: RCV000002947
dbSNP Id: rs120074159

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78407804C>G , CM000666.2:g.78407804C>G GRCh38
NC_000004.11:g.79328958C>G , CM000666.1:g.79328958C>G GRCh37
NC_000004.10:g.79547982C>G NCBI36
NG_015812.1:g.355235C>G
NG_015812.2:g.355235C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000325942.11:c.4271C>G ENSP00000326330.6:p.Ser1424Ter
ENST00000682513.1:c.4271C>G ENSP00000508201.1:p.Ser1424Ter
ENST00000684159.1:c.4271C>G ENSP00000506875.1:p.Ser1424Ter
ENST00000512123.4:c.4271C>G MANE Select ENSP00000422834.2:p.Ser1424Ter
ENST00000264899.10:c.845-36299C>G ENSP00000264899.7:n.845-36299C>G
ENST00000325942.10:c.4271C>G ENSP00000326330.6:p.Ser1424Ter
ENST00000512123.3:c.4271C>G ENSP00000422834.2:p.Ser1424Ter
NM_001166133.1:c.4271C>G NP_001159605.1:p.Ser1424Ter
NM_025074.6:c.4271C>G NP_079350.5:p.Ser1424Ter
XM_006714314.1:c.4271C>G XP_006714377.1:p.Ser1424Ter
XM_006714316.1:c.4271C>G XP_006714379.1:p.Ser1424Ter
XM_011532270.1:c.1970C>G XP_011530572.1:p.Ser657Ter
XM_006714316.3:c.4271C>G XP_006714379.1:p.Ser1424Ter
NM_025074.7:c.4271C>G MANE Select NP_079350.5:p.Ser1424Ter
NM_001166133.2:c.4271C>G NP_001159605.1:p.Ser1424Ter