Canonical Allele Identifier: CA1470477810
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78359539T>G , CM000666.2:g.78359539T>G GRCh38
NC_000004.11:g.79280693T>G , CM000666.1:g.79280693T>G GRCh37
NC_000004.10:g.79499717T>G NCBI36
NG_015812.1:g.306970T>G
NG_015812.2:g.306970T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000325942.11:c.2423-3974T>G ENSP00000326330.6:n.2423-3974T>G
ENST00000682513.1:c.2423-3974T>G ENSP00000508201.1:n.2423-3974T>G
ENST00000684159.1:c.2423-3974T>G ENSP00000506875.1:n.2423-3974T>G
ENST00000512123.4:c.2423-3974T>G MANE Select ENSP00000422834.2:n.2423-3974T>G
ENST00000264899.10:c.845-84564T>G ENSP00000264899.7:n.845-84564T>G
ENST00000325942.10:c.2423-3974T>G ENSP00000326330.6:n.2423-3974T>G
ENST00000512123.3:c.2423-3974T>G ENSP00000422834.2:n.2423-3974T>G
NM_001166133.1:c.2423-3974T>G NP_001159605.1:n.2423-3974T>G
NM_025074.6:c.2423-3974T>G NP_079350.5:n.2423-3974T>G
XM_006714314.1:c.2423-3974T>G XP_006714377.1:n.2423-3974T>G
XM_006714316.1:c.2423-3974T>G XP_006714379.1:n.2423-3974T>G
XM_011532270.1:c.118-3974T>G XP_011530572.1:n.118-3974T>G
XM_006714316.3:c.2423-3974T>G XP_006714379.1:n.2423-3974T>G
NM_025074.7:c.2423-3974T>G MANE Select NP_079350.5:n.2423-3974T>G
NM_001166133.2:c.2423-3974T>G NP_001159605.1:n.2423-3974T>G