Canonical Allele Identifier: CA1698577259

Gene: NT5C3A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33021314G= , CM000669.2:g.33021314G=	GRCh38
NC_000007.13:g.33060926G= , CM000669.1:g.33060926G=	GRCh37
NC_000007.12:g.33027451G=	NCBI36
NG_015800.1:g.46484C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409467.6:c.260C=	ENSP00000387166.1:p.Pro87=
ENST00000610140.7:c.398C= MANE Select	ENSP00000476480.2:p.Pro133=
ENST00000643244.1:c.296C=	ENSP00000496364.1:p.Pro99=
ENST00000242210.11:c.413C=	ENSP00000242210.7:p.Pro138=
ENST00000381626.6:c.260C=	ENSP00000371039.2:p.Pro87=
ENST00000396152.6:c.296C=	ENSP00000379456.2:p.Pro99=
ENST00000405342.5:c.296C=	ENSP00000385261.1:p.Pro99=
ENST00000409467.5:c.260C=	ENSP00000387166.1:p.Pro87=
ENST00000409787.4:c.296C=	ENSP00000387205.1:p.Pro99=
ENST00000456458.5:c.*303C=	ENSP00000389676.2:n.*303C=
ENST00000610140.5:c.398C=	ENSP00000476480.1:p.Pro133=
ENST00000620705.4:c.413C=	ENSP00000484415.1:p.Pro138=
NM_001002009.2:c.296C=	NP_001002009.1:p.Pro99=
NM_001002010.2:c.413C=	NP_001002010.1:p.Pro138=
NM_001166118.2:c.260C=	NP_001159590.1:p.Pro87=
NM_016489.12:c.296C=	NP_057573.2:p.Pro99=
XM_011515409.1:c.260C=	XP_011513711.1:p.Pro87=
NM_001002010.3:c.398C=	NP_001002010.2:p.Pro133=
NM_001356996.1:c.260C=	NP_001343925.1:p.Pro87=
NM_001002009.3:c.296C=	NP_001002009.1:p.Pro99=
NM_001002010.5:c.398C= MANE Select	NP_001002010.2:p.Pro133=
NM_001166118.3:c.260C=	NP_001159590.1:p.Pro87=
NM_001356996.2:c.260C=	NP_001343925.1:p.Pro87=
NM_001374335.1:c.299C=	NP_001361264.1:p.Pro100=
NM_001374336.1:c.260C=	NP_001361265.1:p.Pro87=
NM_001374337.1:c.260C=	NP_001361266.1:p.Pro87=
NM_001374338.1:c.398C=	NP_001361267.1:p.Pro133=
NM_001374339.1:c.197C=	NP_001361268.1:p.Pro66=
NM_016489.13:c.296C=	NP_057573.2:p.Pro99=
NM_001356996.3:c.260C=	NP_001343925.1:p.Pro87=
NM_016489.14:c.296C=	NP_057573.2:p.Pro99=