Canonical Allele Identifier: CA99955783
Community Standard Title: NM_025074.7(FRAS1):c.8604+5G>A
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78481969G>A , CM000666.2:g.78481969G>A GRCh38
NC_000004.11:g.79403123G>A , CM000666.1:g.79403123G>A GRCh37
NC_000004.10:g.79622147G>A NCBI36
NG_015812.1:g.429400G>A
NG_015812.2:g.429400G>A

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.8604+5G>A MANE Select NP_079350.5:n.8604+5G>A
ENST00000512123.4:c.8604+5G>A MANE Select ENSP00000422834.2:n.8604+5G>A
NM_025074.6:c.8604+5G>A NP_079350.5:n.8604+5G>A
ENST00000512123.3:c.8604+5G>A ENSP00000422834.2:n.8604+5G>A
ENST00000682513.1:c.8604+5G>A ENSP00000508201.1:n.8604+5G>A
XM_006714314.1:c.8598+5G>A XP_006714377.1:n.8598+5G>A
XM_006714316.1:c.8376+5G>A XP_006714379.1:n.8376+5G>A
XM_006714316.3:c.8376+5G>A XP_006714379.1:n.8376+5G>A
XM_011532270.1:c.6303+5G>A XP_011530572.1:n.6303+5G>A
XM_011532271.1:c.3492+5G>A XP_011530573.1:n.3492+5G>A