Canonical Allele Identifier: CA5275563
Community Standard Title: NM_000755.5(CRAT):c.961C>T (p.Arg321Cys)
Gene: CRAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129100534G>A , CM000671.2:g.129100534G>A GRCh38
NC_000009.11:g.131862813G>A , CM000671.1:g.131862813G>A GRCh37
NC_000009.10:g.130902634G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_000755.5:c.961C>T MANE Select NP_000746.3:p.Arg321Cys
ENST00000318080.7:c.961C>T MANE Select ENSP00000315013.2:p.Arg321Cys
NM_000755.3:c.961C>T NP_000746.2:p.Arg321Cys
NM_000755.4:c.961C>T NP_000746.2:p.Arg321Cys
NM_001257363.1:c.898C>T NP_001244292.1:p.Arg300Cys
NM_001257363.2:c.898C>T NP_001244292.1:p.Arg300Cys
NM_001257363.3:c.898C>T NP_001244292.2:p.Arg300Cys
NM_001346546.1:c.964C>T NP_001333475.1:p.Arg322Cys
NM_001346546.2:c.964C>T NP_001333475.2:p.Arg322Cys
NM_001346547.1:c.961C>T NP_001333476.1:p.Arg321Cys
NM_001346547.2:c.961C>T NP_001333476.2:p.Arg321Cys
NM_001346548.1:c.898C>T NP_001333477.1:p.Arg300Cys
NM_001346548.2:c.898C>T NP_001333477.2:p.Arg300Cys
NM_001346549.1:c.841C>T NP_001333478.1:p.Arg281Cys
NM_001346549.2:c.841C>T NP_001333478.2:p.Arg281Cys
NM_004003.3:c.898C>T NP_003994.2:p.Arg300Cys
NM_004003.4:c.898C>T NP_003994.3:p.Arg300Cys
ENST00000318080.6:c.961C>T ENSP00000315013.2:p.Arg321Cys
ENST00000455396.2:c.841C>T ENSP00000395458.2:p.Arg281Cys
ENST00000458362.5:c.*937C>T ENSP00000400367.1:n.*937C>T
ENST00000679520.1:c.*1013C>T ENSP00000505259.1:n.*1013C>T
ENST00000679716.1:n.2955C>T
ENST00000680093.1:c.*147C>T ENSP00000506286.1:n.*147C>T
ENST00000680117.1:c.961C>T ENSP00000505542.1:p.Arg321Cys
ENST00000680523.1:n.1243C>T
ENST00000681040.1:c.*937C>T ENSP00000506678.1:n.*937C>T
ENST00000681118.1:n.2427C>T
ENST00000681325.1:c.961C>T ENSP00000506574.1:p.Arg321Cys
ENST00000681622.1:c.*1217C>T ENSP00000505897.1:n.*1217C>T
ENST00000681627.1:c.961C>T ENSP00000506267.1:p.Arg321Cys
ENST00000681689.1:c.*937C>T ENSP00000505435.1:n.*937C>T
ENST00000681725.1:c.961C>T ENSP00000505817.1:p.Arg321Cys
ENST00000681911.1:c.*996C>T ENSP00000506533.1:n.*996C>T
XM_005251706.2:c.964C>T XP_005251763.1:p.Arg322Cys
XM_005251708.2:c.898C>T XP_005251765.1:p.Arg300Cys
XM_005251708.4:c.898C>T XP_005251765.1:p.Arg300Cys
XM_017014275.1:c.964C>T XP_016869764.1:p.Arg322Cys
XM_024447414.1:c.949C>T XP_024303182.1:p.Arg317Cys