Canonical Allele Identifier: CA357374897

Gene: FRAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78375737A>G , CM000666.2:g.78375737A>G	GRCh38
NC_000004.11:g.79296891A>G , CM000666.1:g.79296891A>G	GRCh37
NC_000004.10:g.79515915A>G	NCBI36
NG_015812.1:g.323168A>G
NG_015812.2:g.323168A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025074.7:c.3152-2A>G MANE Select	NP_079350.5:n.3152-2A>G
ENST00000512123.4:c.3152-2A>G MANE Select	ENSP00000422834.2:n.3152-2A>G
NM_001166133.1:c.3152-2A>G	NP_001159605.1:n.3152-2A>G
NM_001166133.2:c.3152-2A>G	NP_001159605.1:n.3152-2A>G
NM_025074.6:c.3152-2A>G	NP_079350.5:n.3152-2A>G
ENST00000264899.10:c.845-68366A>G	ENSP00000264899.7:n.845-68366A>G
ENST00000325942.10:c.3152-2A>G	ENSP00000326330.6:n.3152-2A>G
ENST00000325942.11:c.3152-2A>G	ENSP00000326330.6:n.3152-2A>G
ENST00000512123.3:c.3152-2A>G	ENSP00000422834.2:n.3152-2A>G
ENST00000682513.1:c.3152-2A>G	ENSP00000508201.1:n.3152-2A>G
ENST00000684159.1:c.3152-2A>G	ENSP00000506875.1:n.3152-2A>G
XM_006714314.1:c.3152-2A>G	XP_006714377.1:n.3152-2A>G
XM_006714316.1:c.3152-2A>G	XP_006714379.1:n.3152-2A>G
XM_006714316.3:c.3152-2A>G	XP_006714379.1:n.3152-2A>G
XM_011532270.1:c.851-2A>G	XP_011530572.1:n.851-2A>G