Canonical Allele Identifier: CA2977958

Gene: FRAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78464590G>A , CM000666.2:g.78464590G>A	GRCh38
NC_000004.11:g.79385744G>A , CM000666.1:g.79385744G>A	GRCh37
NC_000004.10:g.79604768G>A	NCBI36
NG_015812.1:g.412021G>A
NG_015812.2:g.412021G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_025074.7:c.7029+7G>A MANE Select	NP_079350.5:n.7029+7G>A
ENST00000512123.4:c.7029+7G>A MANE Select	ENSP00000422834.2:n.7029+7G>A
NM_025074.6:c.7029+7G>A	NP_079350.5:n.7029+7G>A
ENST00000512123.3:c.7029+7G>A	ENSP00000422834.2:n.7029+7G>A
ENST00000682513.1:c.7029+7G>A	ENSP00000508201.1:n.7029+7G>A
XM_006714314.1:c.7023+7G>A	XP_006714377.1:n.7023+7G>A
XM_006714316.1:c.7029+7G>A	XP_006714379.1:n.7029+7G>A
XM_006714316.3:c.7029+7G>A	XP_006714379.1:n.7029+7G>A
XM_011532270.1:c.4728+7G>A	XP_011530572.1:n.4728+7G>A
XM_011532271.1:c.1917+7G>A	XP_011530573.1:n.1917+7G>A