Canonical Allele Identifier: CA357381393
Community Standard Title: NM_025074.7(FRAS1):c.4623C>A (p.Tyr1541Ter)
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78421945C>A , CM000666.2:g.78421945C>A GRCh38
NC_000004.11:g.79343099C>A , CM000666.1:g.79343099C>A GRCh37
NC_000004.10:g.79562123C>A NCBI36
NG_015812.1:g.369376C>A
NG_015812.2:g.369376C>A

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.4623C>A MANE Select NP_079350.5:p.Tyr1541Ter
ENST00000512123.4:c.4623C>A MANE Select ENSP00000422834.2:p.Tyr1541Ter
NM_001166133.1:c.4623C>A NP_001159605.1:p.Tyr1541Ter
NM_001166133.2:c.4623C>A NP_001159605.1:p.Tyr1541Ter
NM_025074.6:c.4623C>A NP_079350.5:p.Tyr1541Ter
ENST00000264899.10:c.845-22158C>A ENSP00000264899.7:n.845-22158C>A
ENST00000325942.10:c.4623C>A ENSP00000326330.6:p.Tyr1541Ter
ENST00000325942.11:c.4623C>A ENSP00000326330.6:p.Tyr1541Ter
ENST00000510944.3:c.27-2443C>A
ENST00000512123.3:c.4623C>A ENSP00000422834.2:p.Tyr1541Ter
ENST00000682513.1:c.4623C>A ENSP00000508201.1:p.Tyr1541Ter
ENST00000684159.1:c.4623C>A ENSP00000506875.1:p.Tyr1541Ter
XM_006714314.1:c.4623C>A XP_006714377.1:p.Tyr1541Ter
XM_006714316.1:c.4623C>A XP_006714379.1:p.Tyr1541Ter
XM_006714316.3:c.4623C>A XP_006714379.1:p.Tyr1541Ter
XM_011532270.1:c.2322C>A XP_011530572.1:p.Tyr774Ter