Canonical Allele Identifier: CA2978381
Community Standard Title: NM_025074.7(FRAS1):c.8460A>G (p.Pro2820=)
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78481820A>G , CM000666.2:g.78481820A>G GRCh38
NC_000004.11:g.79402974A>G , CM000666.1:g.79402974A>G GRCh37
NC_000004.10:g.79621998A>G NCBI36
NG_015812.1:g.429251A>G
NG_015812.2:g.429251A>G

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.8460A>G MANE Select NP_079350.5:p.Pro2820=
ENST00000512123.4:c.8460A>G MANE Select ENSP00000422834.2:p.Pro2820=
NM_025074.6:c.8460A>G NP_079350.5:p.Pro2820=
ENST00000512123.3:c.8460A>G ENSP00000422834.2:p.Pro2820=
ENST00000682513.1:c.8460A>G ENSP00000508201.1:p.Pro2820=
XM_006714314.1:c.8454A>G XP_006714377.1:p.Pro2818=
XM_006714316.1:c.8232A>G XP_006714379.1:p.Pro2744=
XM_006714316.3:c.8232A>G XP_006714379.1:p.Pro2744=
XM_011532270.1:c.6159A>G XP_011530572.1:p.Pro2053=
XM_011532271.1:c.3348A>G XP_011530573.1:p.Pro1116=