Canonical Allele Identifier: CA5275271

Gene: CRAT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.129095574G>A , CM000671.2:g.129095574G>A	GRCh38
NC_000009.11:g.131857853G>A , CM000671.1:g.131857853G>A	GRCh37
NC_000009.10:g.130897674G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_000755.5:c.1704C>T MANE Select	NP_000746.3:p.Pro568=
ENST00000318080.7:c.1704C>T MANE Select	ENSP00000315013.2:p.Pro568=
NM_000755.3:c.1704C>T	NP_000746.2:p.Pro568=
NM_000755.4:c.1704C>T	NP_000746.2:p.Pro568=
NM_001257363.1:c.1641C>T	NP_001244292.1:p.Pro547=
NM_001257363.2:c.1641C>T	NP_001244292.1:p.Pro547=
NM_001257363.3:c.1641C>T	NP_001244292.2:p.Pro547=
NM_001346546.1:c.1707C>T	NP_001333475.1:p.Pro569=
NM_001346546.2:c.1707C>T	NP_001333475.2:p.Pro569=
NM_001346547.1:c.1632C>T	NP_001333476.1:p.Pro544=
NM_001346547.2:c.1632C>T	NP_001333476.2:p.Pro544=
NM_001346548.1:c.1569C>T	NP_001333477.1:p.Pro523=
NM_001346548.2:c.1569C>T	NP_001333477.2:p.Pro523=
NM_001346549.1:c.1584C>T	NP_001333478.1:p.Pro528=
NM_001346549.2:c.1584C>T	NP_001333478.2:p.Pro528=
NM_004003.3:c.1641C>T	NP_003994.2:p.Pro547=
NM_004003.4:c.1641C>T	NP_003994.3:p.Pro547=
ENST00000318080.6:c.1704C>T	ENSP00000315013.2:p.Pro568=
ENST00000455396.1:c.427C>T
ENST00000455396.2:c.1584C>T	ENSP00000395458.2:p.Pro528=
ENST00000458362.5:c.*1680C>T	ENSP00000400367.1:n.*1680C>T
ENST00000467343.1:n.281C>T
ENST00000679520.1:c.*1756C>T	ENSP00000505259.1:n.*1756C>T
ENST00000679716.1:n.3698C>T
ENST00000680093.1:c.*890C>T	ENSP00000506286.1:n.*890C>T
ENST00000680117.1:c.1666-78C>T	ENSP00000505542.1:n.1666-78C>T
ENST00000680523.1:n.2686C>T
ENST00000681040.1:c.*1608C>T	ENSP00000506678.1:n.*1608C>T
ENST00000681118.1:n.3170C>T
ENST00000681325.1:c.1479C>T	ENSP00000506574.1:p.Pro493=
ENST00000681622.1:c.*1960C>T	ENSP00000505897.1:n.*1960C>T
ENST00000681627.1:c.1632C>T	ENSP00000506267.1:p.Pro544=
ENST00000681689.1:c.*1635C>T	ENSP00000505435.1:n.*1635C>T
ENST00000681911.1:c.*1739C>T	ENSP00000506533.1:n.*1739C>T
XM_005251706.2:c.1707C>T	XP_005251763.1:p.Pro569=
XM_005251708.2:c.1641C>T	XP_005251765.1:p.Pro547=
XM_005251708.4:c.1641C>T	XP_005251765.1:p.Pro547=
XM_017014275.1:c.1707C>T	XP_016869764.1:p.Pro569=
XM_024447414.1:c.1692C>T	XP_024303182.1:p.Pro564=