Canonical Allele Identifier: CA2977768
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78450277A>G , CM000666.2:g.78450277A>G GRCh38
NC_000004.11:g.79371431A>G , CM000666.1:g.79371431A>G GRCh37
NC_000004.10:g.79590455A>G NCBI36
NG_015812.1:g.397708A>G
NG_015812.2:g.397708A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682513.1:c.6401A>G ENSP00000508201.1:p.Asn2134Ser
ENST00000684159.1:c.6401A>G ENSP00000506875.1:p.Asn2134Ser
ENST00000512123.4:c.6401A>G MANE Select ENSP00000422834.2:p.Asn2134Ser
ENST00000509802.1:n.386A>G
ENST00000512123.3:c.6401A>G ENSP00000422834.2:p.Asn2134Ser
NM_025074.6:c.6401A>G NP_079350.5:p.Asn2134Ser
XM_006714314.1:c.6395A>G XP_006714377.1:p.Asn2132Ser
XM_006714316.1:c.6401A>G XP_006714379.1:p.Asn2134Ser
XM_011532270.1:c.4100A>G XP_011530572.1:p.Asn1367Ser
XM_011532271.1:c.1289A>G XP_011530573.1:p.Asn430Ser
XM_006714316.3:c.6401A>G XP_006714379.1:p.Asn2134Ser
NM_025074.7:c.6401A>G MANE Select NP_079350.5:p.Asn2134Ser