Canonical Allele Identifier: CA1470475930
Gene: FRAS1 HGNC NCBI

Linked Data

dbSNP Id: rs765245941
gnomAD v4: 4-78379713-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78379713A>T , CM000666.2:g.78379713A>T GRCh38
NC_000004.11:g.79300867A>T , CM000666.1:g.79300867A>T GRCh37
NC_000004.10:g.79519891A>T NCBI36
NG_015812.1:g.327144A>T
NG_015812.2:g.327144A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000325942.11:c.3293-13A>T ENSP00000326330.6:n.3293-13A>T
ENST00000682513.1:c.3293-13A>T ENSP00000508201.1:n.3293-13A>T
ENST00000684159.1:c.3293-13A>T ENSP00000506875.1:n.3293-13A>T
ENST00000512123.4:c.3293-13A>T MANE Select ENSP00000422834.2:n.3293-13A>T
ENST00000264899.10:c.845-64390A>T ENSP00000264899.7:n.845-64390A>T
ENST00000325942.10:c.3293-13A>T ENSP00000326330.6:n.3293-13A>T
ENST00000512123.3:c.3293-13A>T ENSP00000422834.2:n.3293-13A>T
NM_001166133.1:c.3293-13A>T NP_001159605.1:n.3293-13A>T
NM_025074.6:c.3293-13A>T NP_079350.5:n.3293-13A>T
XM_006714314.1:c.3293-13A>T XP_006714377.1:n.3293-13A>T
XM_006714316.1:c.3293-13A>T XP_006714379.1:n.3293-13A>T
XM_011532270.1:c.992-13A>T XP_011530572.1:n.992-13A>T
XM_006714316.3:c.3293-13A>T XP_006714379.1:n.3293-13A>T
NM_025074.7:c.3293-13A>T MANE Select NP_079350.5:n.3293-13A>T
NM_001166133.2:c.3293-13A>T NP_001159605.1:n.3293-13A>T