Canonical Allele Identifier: CA357382414

Gene: FRAS1

Linked Data

• MyVariant Identifiers: chr4:g.79432545G>C (hg19) ; chr4:g.78511391G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78511391G>C , CM000666.2:g.78511391G>C	GRCh38
NC_000004.11:g.79432545G>C , CM000666.1:g.79432545G>C	GRCh37
NC_000004.10:g.79651569G>C	NCBI36
NG_015812.1:g.458822G>C
NG_015812.2:g.458822G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682513.1:c.9898G>C	ENSP00000508201.1:p.Asp3300His
ENST00000512123.4:c.9898G>C MANE Select	ENSP00000422834.2:p.Asp3300His
ENST00000512123.3:c.9898G>C	ENSP00000422834.2:p.Asp3300His
NM_025074.6:c.9898G>C	NP_079350.5:p.Asp3300His
XM_006714314.1:c.9892G>C	XP_006714377.1:p.Asp3298His
XM_006714316.1:c.9670G>C	XP_006714379.1:p.Asp3224His
XM_011532270.1:c.7597G>C	XP_011530572.1:p.Asp2533His
XM_011532271.1:c.4786G>C	XP_011530573.1:p.Asp1596His
XM_006714316.3:c.9670G>C	XP_006714379.1:p.Asp3224His
NM_025074.7:c.9898G>C MANE Select	NP_079350.5:p.Asp3300His