Canonical Allele Identifier: CA2671132745

Gene: FRAS1

Linked Data

• gnomAD v4: 4-78379719-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78379719T>G , CM000666.2:g.78379719T>G	GRCh38
NC_000004.11:g.79300873T>G , CM000666.1:g.79300873T>G	GRCh37
NC_000004.10:g.79519897T>G	NCBI36
NG_015812.1:g.327150T>G
NG_015812.2:g.327150T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000325942.11:c.3293-7T>G	ENSP00000326330.6:n.3293-7T>G
ENST00000682513.1:c.3293-7T>G	ENSP00000508201.1:n.3293-7T>G
ENST00000684159.1:c.3293-7T>G	ENSP00000506875.1:n.3293-7T>G
ENST00000512123.4:c.3293-7T>G MANE Select	ENSP00000422834.2:n.3293-7T>G
ENST00000264899.10:c.845-64384T>G	ENSP00000264899.7:n.845-64384T>G
ENST00000325942.10:c.3293-7T>G	ENSP00000326330.6:n.3293-7T>G
ENST00000512123.3:c.3293-7T>G	ENSP00000422834.2:n.3293-7T>G
NM_001166133.1:c.3293-7T>G	NP_001159605.1:n.3293-7T>G
NM_025074.6:c.3293-7T>G	NP_079350.5:n.3293-7T>G
XM_006714314.1:c.3293-7T>G	XP_006714377.1:n.3293-7T>G
XM_006714316.1:c.3293-7T>G	XP_006714379.1:n.3293-7T>G
XM_011532270.1:c.992-7T>G	XP_011530572.1:n.992-7T>G
XM_006714316.3:c.3293-7T>G	XP_006714379.1:n.3293-7T>G
NM_025074.7:c.3293-7T>G MANE Select	NP_079350.5:n.3293-7T>G
NM_001166133.2:c.3293-7T>G	NP_001159605.1:n.3293-7T>G