Canonical Allele Identifier: CA2975826

Gene: FRAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78066033A>C , CM000666.2:g.78066033A>C	GRCh38
NC_000004.11:g.78987187A>C , CM000666.1:g.78987187A>C	GRCh37
NC_000004.10:g.79206211A>C	NCBI36
NG_015812.1:g.13464A>C
NG_015812.2:g.13464A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_025074.7:c.108+17A>C MANE Select	NP_079350.5:n.108+17A>C
ENST00000512123.4:c.108+17A>C MANE Select	ENSP00000422834.2:n.108+17A>C
NM_001166133.1:c.108+17A>C	NP_001159605.1:n.108+17A>C
NM_001166133.2:c.108+17A>C	NP_001159605.1:n.108+17A>C
NM_025074.6:c.108+17A>C	NP_079350.5:n.108+17A>C
ENST00000264899.10:c.108+17A>C	ENSP00000264899.7:n.108+17A>C
ENST00000325942.10:c.108+17A>C	ENSP00000326330.6:n.108+17A>C
ENST00000325942.11:c.108+17A>C	ENSP00000326330.6:n.108+17A>C
ENST00000502446.6:c.108+17A>C	ENSP00000423645.2:n.108+17A>C
ENST00000508900.2:c.108+17A>C	ENSP00000423809.2:n.108+17A>C
ENST00000508909.5:c.108+17A>C	ENSP00000425583.1:n.108+17A>C
ENST00000512123.3:c.108+17A>C	ENSP00000422834.2:n.108+17A>C
ENST00000682513.1:c.108+17A>C	ENSP00000508201.1:n.108+17A>C
ENST00000683711.1:n.428+17A>C
ENST00000684159.1:c.108+17A>C	ENSP00000506875.1:n.108+17A>C
XM_006714314.1:c.108+17A>C	XP_006714377.1:n.108+17A>C
XM_006714316.1:c.108+17A>C	XP_006714379.1:n.108+17A>C
XM_006714316.3:c.108+17A>C	XP_006714379.1:n.108+17A>C