Canonical Allele Identifier: CA357382423

Gene: FRAS1

Linked Data

• MyVariant Identifiers: chr4:g.79432546A>T (hg19) ; chr4:g.78511392A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78511392A>T , CM000666.2:g.78511392A>T	GRCh38
NC_000004.11:g.79432546A>T , CM000666.1:g.79432546A>T	GRCh37
NC_000004.10:g.79651570A>T	NCBI36
NG_015812.1:g.458823A>T
NG_015812.2:g.458823A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682513.1:c.9899A>T	ENSP00000508201.1:p.Asp3300Val
ENST00000512123.4:c.9899A>T MANE Select	ENSP00000422834.2:p.Asp3300Val
ENST00000512123.3:c.9899A>T	ENSP00000422834.2:p.Asp3300Val
NM_025074.6:c.9899A>T	NP_079350.5:p.Asp3300Val
XM_006714314.1:c.9893A>T	XP_006714377.1:p.Asp3298Val
XM_006714316.1:c.9671A>T	XP_006714379.1:p.Asp3224Val
XM_011532270.1:c.7598A>T	XP_011530572.1:p.Asp2533Val
XM_011532271.1:c.4787A>T	XP_011530573.1:p.Asp1596Val
XM_006714316.3:c.9671A>T	XP_006714379.1:p.Asp3224Val
NM_025074.7:c.9899A>T MANE Select	NP_079350.5:p.Asp3300Val