Canonical Allele Identifier: CA439973841
Community Standard Title: NM_025074.7(FRAS1):c.1371T>C (p.Gly457=)
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78284520T>C , CM000666.2:g.78284520T>C GRCh38
NC_000004.11:g.79205674T>C , CM000666.1:g.79205674T>C GRCh37
NC_000004.10:g.79424698T>C NCBI36
NG_015812.1:g.231951T>C
NG_015812.2:g.231951T>C

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.1371T>C MANE Select NP_079350.5:p.Gly457=
ENST00000512123.4:c.1371T>C MANE Select ENSP00000422834.2:p.Gly457=
NM_001166133.1:c.1371T>C NP_001159605.1:p.Gly457=
NM_001166133.2:c.1371T>C NP_001159605.1:p.Gly457=
NM_025074.6:c.1371T>C NP_079350.5:p.Gly457=
ENST00000264899.10:c.844+17225T>C ENSP00000264899.7:n.844+17225T>C
ENST00000325942.10:c.1371T>C ENSP00000326330.6:p.Gly457=
ENST00000325942.11:c.1371T>C ENSP00000326330.6:p.Gly457=
ENST00000502446.5:c.1157T>C
ENST00000502446.6:c.1371T>C ENSP00000423645.2:p.Gly457=
ENST00000508900.1:c.898T>C
ENST00000508900.2:c.1371T>C ENSP00000423809.2:p.Gly457=
ENST00000512123.3:c.1371T>C ENSP00000422834.2:p.Gly457=
ENST00000682513.1:c.1371T>C ENSP00000508201.1:p.Gly457=
ENST00000682583.1:n.584T>C
ENST00000684159.1:c.1371T>C ENSP00000506875.1:p.Gly457=
XM_006714314.1:c.1371T>C XP_006714377.1:p.Gly457=
XM_006714316.1:c.1371T>C XP_006714379.1:p.Gly457=
XM_006714316.3:c.1371T>C XP_006714379.1:p.Gly457=