Canonical Allele Identifier: CA2976903

Gene: FRAS1

Linked Data

• dbSNP Id: rs765245941
• ExAC: 4:79300867 A / C
• gnomAD v2: 4-79300867-A-C
• gnomAD v4: 4-78379713-A-C
• MyVariant Identifiers: chr4:g.79300867A>C (hg19) ; chr4:g.78379713A>C (hg38)

Genomic Alleles

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

Transcript Alleles

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