Canonical Allele Identifier: CA367190330

Gene: NT5C3A

Linked Data

• MyVariant Identifiers: chr7:g.33055282T>A (hg19) ; chr7:g.33015670T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33015670T>A , CM000669.2:g.33015670T>A	GRCh38
NC_000007.13:g.33055282T>A , CM000669.1:g.33055282T>A	GRCh37
NC_000007.12:g.33021807T>A	NCBI36
NG_015800.1:g.52128A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000409467.6:c.756A>T	ENSP00000387166.1:p.Arg252Ser
ENST00000610140.7:c.894A>T MANE Select	ENSP00000476480.2:p.Arg298Ser
ENST00000643244.1:c.792A>T	ENSP00000496364.1:p.Arg264Ser
ENST00000242210.11:c.909A>T	ENSP00000242210.7:p.Arg303Ser
ENST00000381626.6:c.756A>T	ENSP00000371039.2:p.Arg252Ser
ENST00000396152.6:c.792A>T	ENSP00000379456.2:p.Arg264Ser
ENST00000405342.5:c.792A>T	ENSP00000385261.1:p.Arg264Ser
ENST00000409467.5:c.756A>T	ENSP00000387166.1:p.Arg252Ser
ENST00000456458.5:c.*799A>T	ENSP00000389676.2:n.*799A>T
ENST00000473083.1:n.257A>T
ENST00000610140.5:c.894A>T	ENSP00000476480.1:p.Arg298Ser
ENST00000620705.4:c.909A>T	ENSP00000484415.1:p.Arg303Ser
NM_001002009.2:c.792A>T	NP_001002009.1:p.Arg264Ser
NM_001002010.2:c.909A>T	NP_001002010.1:p.Arg303Ser
NM_001166118.2:c.756A>T	NP_001159590.1:p.Arg252Ser
NM_016489.12:c.792A>T	NP_057573.2:p.Arg264Ser
XM_011515409.1:c.756A>T	XP_011513711.1:p.Arg252Ser
NM_001002010.3:c.894A>T	NP_001002010.2:p.Arg298Ser
NM_001356996.1:c.756A>T	NP_001343925.1:p.Arg252Ser
NM_001002009.3:c.792A>T	NP_001002009.1:p.Arg264Ser
NM_001002010.5:c.894A>T MANE Select	NP_001002010.2:p.Arg298Ser
NM_001166118.3:c.756A>T	NP_001159590.1:p.Arg252Ser
NM_001356996.2:c.756A>T	NP_001343925.1:p.Arg252Ser
NM_001374335.1:c.795A>T	NP_001361264.1:p.Arg265Ser
NM_001374336.1:c.756A>T	NP_001361265.1:p.Arg252Ser
NM_001374337.1:c.756A>T	NP_001361266.1:p.Arg252Ser
NM_001374338.1:c.694-839A>T	NP_001361267.1:n.694-839A>T
NM_001374339.1:c.693A>T	NP_001361268.1:p.Arg231Ser
NM_016489.13:c.792A>T	NP_057573.2:p.Arg264Ser
NM_001356996.3:c.756A>T	NP_001343925.1:p.Arg252Ser
NM_016489.14:c.792A>T	NP_057573.2:p.Arg264Ser