Canonical Allele Identifier: CA2978895
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78515858C>T , CM000666.2:g.78515858C>T GRCh38
NC_000004.11:g.79437012C>T , CM000666.1:g.79437012C>T GRCh37
NC_000004.10:g.79656036C>T NCBI36
NG_015812.1:g.463289C>T
NG_015812.2:g.463289C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000512123.4:c.10234C>T MANE Select ENSP00000422834.2:p.Arg3412Cys
ENST00000512123.3:c.10234C>T ENSP00000422834.2:p.Arg3412Cys
NM_025074.6:c.10234C>T NP_079350.5:p.Arg3412Cys
XM_006714314.1:c.10228C>T XP_006714377.1:p.Arg3410Cys
XM_006714316.1:c.10006C>T XP_006714379.1:p.Arg3336Cys
XM_011532270.1:c.7933C>T XP_011530572.1:p.Arg2645Cys
XM_011532271.1:c.5122C>T XP_011530573.1:p.Arg1708Cys
XM_006714316.3:c.10006C>T XP_006714379.1:p.Arg3336Cys
NM_025074.7:c.10234C>T MANE Select NP_079350.5:p.Arg3412Cys