Canonical Allele Identifier: CA2976202

Gene: FRAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78282865C>T , CM000666.2:g.78282865C>T	GRCh38
NC_000004.11:g.79204019C>T , CM000666.1:g.79204019C>T	GRCh37
NC_000004.10:g.79423043C>T	NCBI36
NG_015812.1:g.230296C>T
NG_015812.2:g.230296C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_025074.7:c.1153C>T MANE Select	NP_079350.5:p.Arg385Ter
ENST00000512123.4:c.1153C>T MANE Select	ENSP00000422834.2:p.Arg385Ter
NM_001166133.1:c.1153C>T	NP_001159605.1:p.Arg385Ter
NM_001166133.2:c.1153C>T	NP_001159605.1:p.Arg385Ter
NM_025074.6:c.1153C>T	NP_079350.5:p.Arg385Ter
ENST00000264899.10:c.844+15570C>T	ENSP00000264899.7:n.844+15570C>T
ENST00000325942.10:c.1153C>T	ENSP00000326330.6:p.Arg385Ter
ENST00000325942.11:c.1153C>T	ENSP00000326330.6:p.Arg385Ter
ENST00000502446.5:c.939C>T
ENST00000502446.6:c.1153C>T	ENSP00000423645.2:p.Arg385Ter
ENST00000508900.1:c.680C>T
ENST00000508900.2:c.1153C>T	ENSP00000423809.2:p.Arg385Ter
ENST00000512123.3:c.1153C>T	ENSP00000422834.2:p.Arg385Ter
ENST00000682513.1:c.1153C>T	ENSP00000508201.1:p.Arg385Ter
ENST00000682583.1:n.366C>T
ENST00000683711.1:n.1473C>T
ENST00000684159.1:c.1153C>T	ENSP00000506875.1:p.Arg385Ter
XM_006714314.1:c.1153C>T	XP_006714377.1:p.Arg385Ter
XM_006714316.1:c.1153C>T	XP_006714379.1:p.Arg385Ter
XM_006714316.3:c.1153C>T	XP_006714379.1:p.Arg385Ter