Canonical Allele Identifier: CA5275242
Community Standard Title: NM_000755.5(CRAT):c.1797C>T (p.Asn599=)
Gene: CRAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129095481G>A , CM000671.2:g.129095481G>A GRCh38
NC_000009.11:g.131857760G>A , CM000671.1:g.131857760G>A GRCh37
NC_000009.10:g.130897581G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_000755.5:c.1797C>T MANE Select NP_000746.3:p.Asn599=
ENST00000318080.7:c.1797C>T MANE Select ENSP00000315013.2:p.Asn599=
NM_000755.3:c.1797C>T NP_000746.2:p.Asn599=
NM_000755.4:c.1797C>T NP_000746.2:p.Asn599=
NM_001257363.1:c.1734C>T NP_001244292.1:p.Asn578=
NM_001257363.2:c.1734C>T NP_001244292.1:p.Asn578=
NM_001257363.3:c.1734C>T NP_001244292.2:p.Asn578=
NM_001346546.1:c.1800C>T NP_001333475.1:p.Asn600=
NM_001346546.2:c.1800C>T NP_001333475.2:p.Asn600=
NM_001346547.1:c.1725C>T NP_001333476.1:p.Asn575=
NM_001346547.2:c.1725C>T NP_001333476.2:p.Asn575=
NM_001346548.1:c.1662C>T NP_001333477.1:p.Asn554=
NM_001346548.2:c.1662C>T NP_001333477.2:p.Asn554=
NM_001346549.1:c.1677C>T NP_001333478.1:p.Asn559=
NM_001346549.2:c.1677C>T NP_001333478.2:p.Asn559=
NM_004003.3:c.1734C>T NP_003994.2:p.Asn578=
NM_004003.4:c.1734C>T NP_003994.3:p.Asn578=
ENST00000318080.6:c.1797C>T ENSP00000315013.2:p.Asn599=
ENST00000455396.1:c.520C>T
ENST00000455396.2:c.1677C>T ENSP00000395458.2:p.Asn559=
ENST00000458362.5:c.*1773C>T ENSP00000400367.1:n.*1773C>T
ENST00000467343.1:n.374C>T
ENST00000679520.1:c.*1849C>T ENSP00000505259.1:n.*1849C>T
ENST00000679716.1:n.3791C>T
ENST00000680093.1:c.*983C>T ENSP00000506286.1:n.*983C>T
ENST00000680117.1:c.1681C>T ENSP00000505542.1:p.Arg561Cys
ENST00000680523.1:n.2779C>T
ENST00000681040.1:c.*1701C>T ENSP00000506678.1:n.*1701C>T
ENST00000681118.1:n.3263C>T
ENST00000681325.1:c.1572C>T ENSP00000506574.1:p.Asn524=
ENST00000681622.1:c.*2053C>T ENSP00000505897.1:n.*2053C>T
ENST00000681627.1:c.1725C>T ENSP00000506267.1:p.Asn575=
ENST00000681689.1:c.*1728C>T ENSP00000505435.1:n.*1728C>T
ENST00000681911.1:c.*1832C>T ENSP00000506533.1:n.*1832C>T
XM_005251706.2:c.1800C>T XP_005251763.1:p.Asn600=
XM_005251708.2:c.1734C>T XP_005251765.1:p.Asn578=
XM_005251708.4:c.1734C>T XP_005251765.1:p.Asn578=
XM_017014275.1:c.1800C>T XP_016869764.1:p.Asn600=
XM_024447414.1:c.1785C>T XP_024303182.1:p.Asn595=