Canonical Allele Identifier: CA357368288

Gene: FRAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78317456C>G , CM000666.2:g.78317456C>G	GRCh38
NC_000004.11:g.79238610C>G , CM000666.1:g.79238610C>G	GRCh37
NC_000004.10:g.79457634C>G	NCBI36
NG_015812.1:g.264887C>G
NG_015812.2:g.264887C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325942.11:c.1908C>G	ENSP00000326330.6:p.His636Gln
ENST00000502446.6:c.1908C>G	ENSP00000423645.2:p.His636Gln
ENST00000508900.2:c.1908C>G	ENSP00000423809.2:p.His636Gln
ENST00000682513.1:c.1908C>G	ENSP00000508201.1:p.His636Gln
ENST00000682583.1:n.1134C>G
ENST00000684159.1:c.1908C>G	ENSP00000506875.1:p.His636Gln
ENST00000512123.4:c.1908C>G MANE Select	ENSP00000422834.2:p.His636Gln
ENST00000264899.10:c.844+50161C>G	ENSP00000264899.7:n.844+50161C>G
ENST00000325942.10:c.1908C>G	ENSP00000326330.6:p.His636Gln
ENST00000502446.5:c.1694C>G
ENST00000508900.1:c.1435C>G
ENST00000512123.3:c.1908C>G	ENSP00000422834.2:p.His636Gln
NM_001166133.1:c.1908C>G	NP_001159605.1:p.His636Gln
NM_025074.6:c.1908C>G	NP_079350.5:p.His636Gln
XM_006714314.1:c.1908C>G	XP_006714377.1:p.His636Gln
XM_006714316.1:c.1908C>G	XP_006714379.1:p.His636Gln
XM_006714316.3:c.1908C>G	XP_006714379.1:p.His636Gln
NM_025074.7:c.1908C>G MANE Select	NP_079350.5:p.His636Gln
NM_001166133.2:c.1908C>G	NP_001159605.1:p.His636Gln