Canonical Allele Identifier: CA2977501
Community Standard Title: NM_025074.7(FRAS1):c.5370C>G (p.Tyr1790Ter)
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78438905C>G , CM000666.2:g.78438905C>G GRCh38
NC_000004.11:g.79360059C>G , CM000666.1:g.79360059C>G GRCh37
NC_000004.10:g.79579083C>G NCBI36
NG_015812.1:g.386336C>G
NG_015812.2:g.386336C>G

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.5370C>G MANE Select NP_079350.5:p.Tyr1790Ter
ENST00000512123.4:c.5370C>G MANE Select ENSP00000422834.2:p.Tyr1790Ter
NM_001166133.1:c.5370C>G NP_001159605.1:p.Tyr1790Ter
NM_001166133.2:c.5370C>G NP_001159605.1:p.Tyr1790Ter
NM_025074.6:c.5370C>G NP_079350.5:p.Tyr1790Ter
ENST00000264899.10:c.845-5198C>G ENSP00000264899.7:n.845-5198C>G
ENST00000325942.10:c.5370C>G ENSP00000326330.6:p.Tyr1790Ter
ENST00000325942.11:c.5370C>G ENSP00000326330.6:p.Tyr1790Ter
ENST00000510944.3:c.718C>G
ENST00000512123.3:c.5370C>G ENSP00000422834.2:p.Tyr1790Ter
ENST00000682513.1:c.5370C>G ENSP00000508201.1:p.Tyr1790Ter
ENST00000684159.1:c.5370C>G ENSP00000506875.1:p.Tyr1790Ter
XM_006714314.1:c.5364C>G XP_006714377.1:p.Tyr1788Ter
XM_006714316.1:c.5370C>G XP_006714379.1:p.Tyr1790Ter
XM_006714316.3:c.5370C>G XP_006714379.1:p.Tyr1790Ter
XM_011532270.1:c.3069C>G XP_011530572.1:p.Tyr1023Ter
XM_011532271.1:c.258C>G XP_011530573.1:p.Tyr86Ter