Canonical Allele Identifier: CA915943078
Community Standard Title: NM_025074.7(FRAS1):c.10808+9A>G
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78522817A>G , CM000666.2:g.78522817A>G GRCh38
NC_000004.11:g.79443971A>G , CM000666.1:g.79443971A>G GRCh37
NC_000004.10:g.79662995A>G NCBI36
NG_015812.1:g.470248A>G
NG_015812.2:g.470248A>G

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.10808+9A>G MANE Select NP_079350.5:n.10808+9A>G
ENST00000512123.4:c.10808+9A>G MANE Select ENSP00000422834.2:n.10808+9A>G
NM_025074.6:c.10808+9A>G NP_079350.5:n.10808+9A>G
ENST00000512123.3:c.10808+9A>G ENSP00000422834.2:n.10808+9A>G
XM_006714314.1:c.10802+9A>G XP_006714377.1:n.10802+9A>G
XM_006714316.1:c.10580+9A>G XP_006714379.1:n.10580+9A>G
XM_006714316.3:c.10580+9A>G XP_006714379.1:n.10580+9A>G
XM_011532270.1:c.8507+9A>G XP_011530572.1:n.8507+9A>G
XM_011532271.1:c.5696+9A>G XP_011530573.1:n.5696+9A>G