Canonical Allele Identifier: CA5275270

Gene: CRAT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.129095573C>T , CM000671.2:g.129095573C>T	GRCh38
NC_000009.11:g.131857852C>T , CM000671.1:g.131857852C>T	GRCh37
NC_000009.10:g.130897673C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_000755.5:c.1705G>A MANE Select	NP_000746.3:p.Val569Met
ENST00000318080.7:c.1705G>A MANE Select	ENSP00000315013.2:p.Val569Met
NM_000755.3:c.1705G>A	NP_000746.2:p.Val569Met
NM_000755.4:c.1705G>A	NP_000746.2:p.Val569Met
NM_001257363.1:c.1642G>A	NP_001244292.1:p.Val548Met
NM_001257363.2:c.1642G>A	NP_001244292.1:p.Val548Met
NM_001257363.3:c.1642G>A	NP_001244292.2:p.Val548Met
NM_001346546.1:c.1708G>A	NP_001333475.1:p.Val570Met
NM_001346546.2:c.1708G>A	NP_001333475.2:p.Val570Met
NM_001346547.1:c.1633G>A	NP_001333476.1:p.Val545Met
NM_001346547.2:c.1633G>A	NP_001333476.2:p.Val545Met
NM_001346548.1:c.1570G>A	NP_001333477.1:p.Val524Met
NM_001346548.2:c.1570G>A	NP_001333477.2:p.Val524Met
NM_001346549.1:c.1585G>A	NP_001333478.1:p.Val529Met
NM_001346549.2:c.1585G>A	NP_001333478.2:p.Val529Met
NM_004003.3:c.1642G>A	NP_003994.2:p.Val548Met
NM_004003.4:c.1642G>A	NP_003994.3:p.Val548Met
ENST00000318080.6:c.1705G>A	ENSP00000315013.2:p.Val569Met
ENST00000455396.1:c.428G>A
ENST00000455396.2:c.1585G>A	ENSP00000395458.2:p.Val529Met
ENST00000458362.5:c.*1681G>A	ENSP00000400367.1:n.*1681G>A
ENST00000467343.1:n.282G>A
ENST00000679520.1:c.*1757G>A	ENSP00000505259.1:n.*1757G>A
ENST00000679716.1:n.3699G>A
ENST00000680093.1:c.*891G>A	ENSP00000506286.1:n.*891G>A
ENST00000680117.1:c.1666-77G>A	ENSP00000505542.1:n.1666-77G>A
ENST00000680523.1:n.2687G>A
ENST00000681040.1:c.*1609G>A	ENSP00000506678.1:n.*1609G>A
ENST00000681118.1:n.3171G>A
ENST00000681325.1:c.1480G>A	ENSP00000506574.1:p.Val494Met
ENST00000681622.1:c.*1961G>A	ENSP00000505897.1:n.*1961G>A
ENST00000681627.1:c.1633G>A	ENSP00000506267.1:p.Val545Met
ENST00000681689.1:c.*1636G>A	ENSP00000505435.1:n.*1636G>A
ENST00000681911.1:c.*1740G>A	ENSP00000506533.1:n.*1740G>A
XM_005251706.2:c.1708G>A	XP_005251763.1:p.Val570Met
XM_005251708.2:c.1642G>A	XP_005251765.1:p.Val548Met
XM_005251708.4:c.1642G>A	XP_005251765.1:p.Val548Met
XM_017014275.1:c.1708G>A	XP_016869764.1:p.Val570Met
XM_024447414.1:c.1693G>A	XP_024303182.1:p.Val565Met