Canonical Allele Identifier: CA357375509

Gene: FRAS1

Linked Data

• ClinVar Variation Id: 1332873
• ClinVar RCV Id: RCV001806447
• dbSNP Id: rs2110319166
• MyVariant Identifiers: chr4:g.79300878A>T (hg19) ; chr4:g.78379724A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78379724A>T , CM000666.2:g.78379724A>T	GRCh38
NC_000004.11:g.79300878A>T , CM000666.1:g.79300878A>T	GRCh37
NC_000004.10:g.79519902A>T	NCBI36
NG_015812.1:g.327155A>T
NG_015812.2:g.327155A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000325942.11:c.3293-2A>T	ENSP00000326330.6:n.3293-2A>T
ENST00000682513.1:c.3293-2A>T	ENSP00000508201.1:n.3293-2A>T
ENST00000684159.1:c.3293-2A>T	ENSP00000506875.1:n.3293-2A>T
ENST00000512123.4:c.3293-2A>T MANE Select	ENSP00000422834.2:n.3293-2A>T
ENST00000264899.10:c.845-64379A>T	ENSP00000264899.7:n.845-64379A>T
ENST00000325942.10:c.3293-2A>T	ENSP00000326330.6:n.3293-2A>T
ENST00000512123.3:c.3293-2A>T	ENSP00000422834.2:n.3293-2A>T
NM_001166133.1:c.3293-2A>T	NP_001159605.1:n.3293-2A>T
NM_025074.6:c.3293-2A>T	NP_079350.5:n.3293-2A>T
XM_006714314.1:c.3293-2A>T	XP_006714377.1:n.3293-2A>T
XM_006714316.1:c.3293-2A>T	XP_006714379.1:n.3293-2A>T
XM_011532270.1:c.992-2A>T	XP_011530572.1:n.992-2A>T
XM_006714316.3:c.3293-2A>T	XP_006714379.1:n.3293-2A>T
NM_025074.7:c.3293-2A>T MANE Select	NP_079350.5:n.3293-2A>T
NM_001166133.2:c.3293-2A>T	NP_001159605.1:n.3293-2A>T