Canonical Allele Identifier: CA357382078

Gene: FRAS1

Linked Data

• dbSNP Id: rs1721028949
• MyVariant Identifiers: chr4:g.79432463T>G (hg19) ; chr4:g.78511309T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78511309T>G , CM000666.2:g.78511309T>G	GRCh38
NC_000004.11:g.79432463T>G , CM000666.1:g.79432463T>G	GRCh37
NC_000004.10:g.79651487T>G	NCBI36
NG_015812.1:g.458740T>G
NG_015812.2:g.458740T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682513.1:c.9816T>G	ENSP00000508201.1:p.His3272Gln
ENST00000512123.4:c.9816T>G MANE Select	ENSP00000422834.2:p.His3272Gln
ENST00000512123.3:c.9816T>G	ENSP00000422834.2:p.His3272Gln
NM_025074.6:c.9816T>G	NP_079350.5:p.His3272Gln
XM_006714314.1:c.9810T>G	XP_006714377.1:p.His3270Gln
XM_006714316.1:c.9588T>G	XP_006714379.1:p.His3196Gln
XM_011532270.1:c.7515T>G	XP_011530572.1:p.His2505Gln
XM_011532271.1:c.4704T>G	XP_011530573.1:p.His1568Gln
XM_006714316.3:c.9588T>G	XP_006714379.1:p.His3196Gln
NM_025074.7:c.9816T>G MANE Select	NP_079350.5:p.His3272Gln