Canonical Allele Identifier: CA2977933
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78464479G>C , CM000666.2:g.78464479G>C GRCh38
NC_000004.11:g.79385633G>C , CM000666.1:g.79385633G>C GRCh37
NC_000004.10:g.79604657G>C NCBI36
NG_015812.1:g.411910G>C
NG_015812.2:g.411910G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682513.1:c.6925G>C ENSP00000508201.1:p.Asp2309His
ENST00000512123.4:c.6925G>C MANE Select ENSP00000422834.2:p.Asp2309His
ENST00000512123.3:c.6925G>C ENSP00000422834.2:p.Asp2309His
NM_025074.6:c.6925G>C NP_079350.5:p.Asp2309His
XM_006714314.1:c.6919G>C XP_006714377.1:p.Asp2307His
XM_006714316.1:c.6925G>C XP_006714379.1:p.Asp2309His
XM_011532270.1:c.4624G>C XP_011530572.1:p.Asp1542His
XM_011532271.1:c.1813G>C XP_011530573.1:p.Asp605His
XM_006714316.3:c.6925G>C XP_006714379.1:p.Asp2309His
NM_025074.7:c.6925G>C MANE Select NP_079350.5:p.Asp2309His