Canonical Allele Identifier: CA2976764

Gene: FRAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78372713T>C , CM000666.2:g.78372713T>C	GRCh38
NC_000004.11:g.79293867T>C , CM000666.1:g.79293867T>C	GRCh37
NC_000004.10:g.79512891T>C	NCBI36
NG_015812.1:g.320144T>C
NG_015812.2:g.320144T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_025074.7:c.2870-5T>C MANE Select	NP_079350.5:n.2870-5T>C
ENST00000512123.4:c.2870-5T>C MANE Select	ENSP00000422834.2:n.2870-5T>C
NM_001166133.1:c.2870-5T>C	NP_001159605.1:n.2870-5T>C
NM_001166133.2:c.2870-5T>C	NP_001159605.1:n.2870-5T>C
NM_025074.6:c.2870-5T>C	NP_079350.5:n.2870-5T>C
ENST00000264899.10:c.845-71390T>C	ENSP00000264899.7:n.845-71390T>C
ENST00000325942.10:c.2870-5T>C	ENSP00000326330.6:n.2870-5T>C
ENST00000325942.11:c.2870-5T>C	ENSP00000326330.6:n.2870-5T>C
ENST00000512123.3:c.2870-5T>C	ENSP00000422834.2:n.2870-5T>C
ENST00000682513.1:c.2870-5T>C	ENSP00000508201.1:n.2870-5T>C
ENST00000684159.1:c.2870-5T>C	ENSP00000506875.1:n.2870-5T>C
XM_006714314.1:c.2870-5T>C	XP_006714377.1:n.2870-5T>C
XM_006714316.1:c.2870-5T>C	XP_006714379.1:n.2870-5T>C
XM_006714316.3:c.2870-5T>C	XP_006714379.1:n.2870-5T>C
XM_011532270.1:c.569-5T>C	XP_011530572.1:n.569-5T>C