Canonical Allele Identifier: CA2580071806

Gene: FRAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78058104G>T , CM000666.2:g.78058104G>T	GRCh38
NC_000004.11:g.78979258G>T , CM000666.1:g.78979258G>T	GRCh37
NC_000004.10:g.79198282G>T	NCBI36
NG_015812.1:g.5535G>T
NG_015812.2:g.5535G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_025074.7:c.76+19G>T MANE Select	NP_079350.5:n.76+19G>T
ENST00000512123.4:c.76+19G>T MANE Select	ENSP00000422834.2:n.76+19G>T
NM_001166133.1:c.76+19G>T	NP_001159605.1:n.76+19G>T
NM_001166133.2:c.76+19G>T	NP_001159605.1:n.76+19G>T
NM_025074.6:c.76+19G>T	NP_079350.5:n.76+19G>T
ENST00000264899.10:c.76+19G>T	ENSP00000264899.7:n.76+19G>T
ENST00000325942.10:c.76+19G>T	ENSP00000326330.6:n.76+19G>T
ENST00000325942.11:c.76+19G>T	ENSP00000326330.6:n.76+19G>T
ENST00000502446.6:c.76+19G>T	ENSP00000423645.2:n.76+19G>T
ENST00000508900.2:c.76+19G>T	ENSP00000423809.2:n.76+19G>T
ENST00000508909.5:c.76+19G>T	ENSP00000425583.1:n.76+19G>T
ENST00000512123.3:c.76+19G>T	ENSP00000422834.2:n.76+19G>T
ENST00000682513.1:c.76+19G>T	ENSP00000508201.1:n.76+19G>T
ENST00000683711.1:n.396+19G>T
ENST00000684159.1:c.76+19G>T	ENSP00000506875.1:n.76+19G>T
XM_006714314.1:c.76+19G>T	XP_006714377.1:n.76+19G>T
XM_006714316.1:c.76+19G>T	XP_006714379.1:n.76+19G>T
XM_006714316.3:c.76+19G>T	XP_006714379.1:n.76+19G>T