Canonical Allele Identifier: CA357382199

Gene: FRAS1

Linked Data

• MyVariant Identifiers: chr4:g.79432488G>C (hg19) ; chr4:g.78511334G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78511334G>C , CM000666.2:g.78511334G>C	GRCh38
NC_000004.11:g.79432488G>C , CM000666.1:g.79432488G>C	GRCh37
NC_000004.10:g.79651512G>C	NCBI36
NG_015812.1:g.458765G>C
NG_015812.2:g.458765G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682513.1:c.9841G>C	ENSP00000508201.1:p.Asp3281His
ENST00000512123.4:c.9841G>C MANE Select	ENSP00000422834.2:p.Asp3281His
ENST00000512123.3:c.9841G>C	ENSP00000422834.2:p.Asp3281His
NM_025074.6:c.9841G>C	NP_079350.5:p.Asp3281His
XM_006714314.1:c.9835G>C	XP_006714377.1:p.Asp3279His
XM_006714316.1:c.9613G>C	XP_006714379.1:p.Asp3205His
XM_011532270.1:c.7540G>C	XP_011530572.1:p.Asp2514His
XM_011532271.1:c.4729G>C	XP_011530573.1:p.Asp1577His
XM_006714316.3:c.9613G>C	XP_006714379.1:p.Asp3205His
NM_025074.7:c.9841G>C MANE Select	NP_079350.5:p.Asp3281His