Canonical Allele Identifier: CA2832541969

Gene: FRAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78407748dup , CM000666.2:g.78407748dup	GRCh38
NC_000004.11:g.79328902dup , CM000666.1:g.79328902dup	GRCh37
NC_000004.10:g.79547926dup	NCBI36
NG_015812.1:g.355179dup
NG_015812.2:g.355179dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325942.11:c.4215dup	ENSP00000326330.6:p.Thr1406HisfsTer11
ENST00000682513.1:c.4215dup	ENSP00000508201.1:p.Thr1406HisfsTer11
ENST00000684159.1:c.4215dup	ENSP00000506875.1:p.Thr1406HisfsTer11
ENST00000512123.4:c.4215dup MANE Select	ENSP00000422834.2:p.Thr1406HisfsTer11
ENST00000264899.10:c.845-36355dup	ENSP00000264899.7:n.845-36355dup
ENST00000325942.10:c.4215dup	ENSP00000326330.6:p.Thr1406HisfsTer11
ENST00000512123.3:c.4215dup	ENSP00000422834.2:p.Thr1406HisfsTer11
NM_001166133.1:c.4215dup	NP_001159605.1:p.Thr1406HisfsTer11
NM_025074.6:c.4215dup	NP_079350.5:p.Thr1406HisfsTer11
XM_006714314.1:c.4215dup	XP_006714377.1:p.Thr1406HisfsTer11
XM_006714316.1:c.4215dup	XP_006714379.1:p.Thr1406HisfsTer11
XM_011532270.1:c.1914dup	XP_011530572.1:p.Thr639HisfsTer11
XM_006714316.3:c.4215dup	XP_006714379.1:p.Thr1406HisfsTer11
NM_025074.7:c.4215dup MANE Select	NP_079350.5:p.Thr1406HisfsTer11
NM_001166133.2:c.4215dup	NP_001159605.1:p.Thr1406HisfsTer11