Canonical Allele Identifier: CA2671132741

Gene: FRAS1

Linked Data

• gnomAD v4: 4-78379712-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78379712C>A , CM000666.2:g.78379712C>A	GRCh38
NC_000004.11:g.79300866C>A , CM000666.1:g.79300866C>A	GRCh37
NC_000004.10:g.79519890C>A	NCBI36
NG_015812.1:g.327143C>A
NG_015812.2:g.327143C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000325942.11:c.3293-14C>A	ENSP00000326330.6:n.3293-14C>A
ENST00000682513.1:c.3293-14C>A	ENSP00000508201.1:n.3293-14C>A
ENST00000684159.1:c.3293-14C>A	ENSP00000506875.1:n.3293-14C>A
ENST00000512123.4:c.3293-14C>A MANE Select	ENSP00000422834.2:n.3293-14C>A
ENST00000264899.10:c.845-64391C>A	ENSP00000264899.7:n.845-64391C>A
ENST00000325942.10:c.3293-14C>A	ENSP00000326330.6:n.3293-14C>A
ENST00000512123.3:c.3293-14C>A	ENSP00000422834.2:n.3293-14C>A
NM_001166133.1:c.3293-14C>A	NP_001159605.1:n.3293-14C>A
NM_025074.6:c.3293-14C>A	NP_079350.5:n.3293-14C>A
XM_006714314.1:c.3293-14C>A	XP_006714377.1:n.3293-14C>A
XM_006714316.1:c.3293-14C>A	XP_006714379.1:n.3293-14C>A
XM_011532270.1:c.992-14C>A	XP_011530572.1:n.992-14C>A
XM_006714316.3:c.3293-14C>A	XP_006714379.1:n.3293-14C>A
NM_025074.7:c.3293-14C>A MANE Select	NP_079350.5:n.3293-14C>A
NM_001166133.2:c.3293-14C>A	NP_001159605.1:n.3293-14C>A