Canonical Allele Identifier: CA2977925
Community Standard Title: NM_025074.7(FRAS1):c.6889-9C>G
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78464434C>G , CM000666.2:g.78464434C>G GRCh38
NC_000004.11:g.79385588C>G , CM000666.1:g.79385588C>G GRCh37
NC_000004.10:g.79604612C>G NCBI36
NG_015812.1:g.411865C>G
NG_015812.2:g.411865C>G

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.6889-9C>G MANE Select NP_079350.5:n.6889-9C>G
ENST00000512123.4:c.6889-9C>G MANE Select ENSP00000422834.2:n.6889-9C>G
NM_025074.6:c.6889-9C>G NP_079350.5:n.6889-9C>G
ENST00000512123.3:c.6889-9C>G ENSP00000422834.2:n.6889-9C>G
ENST00000682513.1:c.6889-9C>G ENSP00000508201.1:n.6889-9C>G
XM_006714314.1:c.6883-9C>G XP_006714377.1:n.6883-9C>G
XM_006714316.1:c.6889-9C>G XP_006714379.1:n.6889-9C>G
XM_006714316.3:c.6889-9C>G XP_006714379.1:n.6889-9C>G
XM_011532270.1:c.4588-9C>G XP_011530572.1:n.4588-9C>G
XM_011532271.1:c.1777-9C>G XP_011530573.1:n.1777-9C>G