Canonical Allele Identifier: CA439981780
Community Standard Title: NM_025074.7(FRAS1):c.9435G>A (p.Val3145=)
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78507539G>A , CM000666.2:g.78507539G>A GRCh38
NC_000004.11:g.79428693G>A , CM000666.1:g.79428693G>A GRCh37
NC_000004.10:g.79647717G>A NCBI36
NG_015812.1:g.454970G>A
NG_015812.2:g.454970G>A

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.9435G>A MANE Select NP_079350.5:p.Val3145=
ENST00000512123.4:c.9435G>A MANE Select ENSP00000422834.2:p.Val3145=
NM_025074.6:c.9435G>A NP_079350.5:p.Val3145=
ENST00000512123.3:c.9435G>A ENSP00000422834.2:p.Val3145=
ENST00000682513.1:c.9435G>A ENSP00000508201.1:p.Val3145=
XM_006714314.1:c.9429G>A XP_006714377.1:p.Val3143=
XM_006714316.1:c.9207G>A XP_006714379.1:p.Val3069=
XM_006714316.3:c.9207G>A XP_006714379.1:p.Val3069=
XM_011532270.1:c.7134G>A XP_011530572.1:p.Val2378=
XM_011532271.1:c.4323G>A XP_011530573.1:p.Val1441=