Canonical Allele Identifier: CA1698574676

Gene: NT5C3A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33015659T= , CM000669.2:g.33015659T=	GRCh38
NC_000007.13:g.33055271T= , CM000669.1:g.33055271T=	GRCh37
NC_000007.12:g.33021796T=	NCBI36
NG_015800.1:g.52139A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000409467.6:c.756+11A=	ENSP00000387166.1:n.756+11A=
ENST00000610140.7:c.894+11A= MANE Select	ENSP00000476480.2:n.894+11A=
ENST00000643244.1:c.792+11A=	ENSP00000496364.1:n.792+11A=
ENST00000242210.11:c.909+11A=	ENSP00000242210.7:n.909+11A=
ENST00000381626.6:c.756+11A=	ENSP00000371039.2:n.756+11A=
ENST00000396152.6:c.792+11A=	ENSP00000379456.2:n.792+11A=
ENST00000405342.5:c.792+11A=	ENSP00000385261.1:n.792+11A=
ENST00000409467.5:c.756+11A=	ENSP00000387166.1:n.756+11A=
ENST00000456458.5:c.*799+11A=	ENSP00000389676.2:n.*799+11A=
ENST00000473083.1:n.257+11A=
ENST00000610140.5:c.894+11A=	ENSP00000476480.1:n.894+11A=
ENST00000620705.4:c.909+11A=	ENSP00000484415.1:n.909+11A=
NM_001002009.2:c.792+11A=	NP_001002009.1:n.792+11A=
NM_001002010.2:c.909+11A=	NP_001002010.1:n.909+11A=
NM_001166118.2:c.756+11A=	NP_001159590.1:n.756+11A=
NM_016489.12:c.792+11A=	NP_057573.2:n.792+11A=
XM_011515409.1:c.756+11A=	XP_011513711.1:n.756+11A=
NM_001002010.3:c.894+11A=	NP_001002010.2:n.894+11A=
NM_001356996.1:c.756+11A=	NP_001343925.1:n.756+11A=
NM_001002009.3:c.792+11A=	NP_001002009.1:n.792+11A=
NM_001002010.5:c.894+11A= MANE Select	NP_001002010.2:n.894+11A=
NM_001166118.3:c.756+11A=	NP_001159590.1:n.756+11A=
NM_001356996.2:c.756+11A=	NP_001343925.1:n.756+11A=
NM_001374335.1:c.795+11A=	NP_001361264.1:n.795+11A=
NM_001374336.1:c.756+11A=	NP_001361265.1:n.756+11A=
NM_001374337.1:c.756+11A=	NP_001361266.1:n.756+11A=
NM_001374338.1:c.694-828A=	NP_001361267.1:n.694-828A=
NM_001374339.1:c.693+11A=	NP_001361268.1:n.693+11A=
NM_016489.13:c.792+11A=	NP_057573.2:n.792+11A=
NM_001356996.3:c.756+11A=	NP_001343925.1:n.756+11A=
NM_016489.14:c.792+11A=	NP_057573.2:n.792+11A=