Canonical Allele Identifier: CA1918678346

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362100G= , CM000672.2:g.71362100G=	GRCh38
NC_000010.10:g.73121857G= , CM000672.1:g.73121857G=	GRCh37
NC_000010.9:g.72791863G=	NCBI36
NG_017066.1:g.47848G=
NG_017066.2:g.47842G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2396G=
ENST00000373189.6:c.920G= MANE Select	ENSP00000362285.5:p.Ser307=
ENST00000479577.2:c.686G=	ENSP00000493995.1:p.Ser229=
ENST00000642198.1:c.*492G=	ENSP00000494827.1:n.*492G=
ENST00000642772.1:c.*94+5857G=	ENSP00000495041.1:n.*94+5857G=
ENST00000643042.1:c.541G=	ENSP00000496674.1:n.541G=
ENST00000643619.1:c.*503G=	ENSP00000494378.1:n.*503G=
ENST00000643752.1:c.*246G=	ENSP00000495000.1:n.*246G=
ENST00000644088.1:c.*241G=	ENSP00000494066.1:n.*241G=
ENST00000644591.1:c.*246G=	ENSP00000496664.1:n.*246G=
ENST00000644895.1:c.*99+5857G=	ENSP00000493872.1:n.*99+5857G=
ENST00000645345.1:c.*492G=	ENSP00000495859.1:n.*492G=
ENST00000647524.1:c.*503G=	ENSP00000495077.1:n.*503G=
ENST00000373189.5:c.920G=	ENSP00000362285.5:p.Ser307=
ENST00000469204.1:n.417G=
NM_001174098.1:c.*149G=	NP_001167569.1:n.*149G=
NM_018344.5:c.920G=	NP_060814.4:p.Ser307=
NR_033413.1:n.894G=
NR_033414.1:n.667G=
XM_006717910.2:c.686G=	XP_006717973.1:p.Ser229=
NM_001363518.1:c.686G=	NP_001350447.1:p.Ser229=
XM_017016377.2:c.482G=	XP_016871866.1:p.Ser161=
XM_017016378.2:c.302G=	XP_016871867.1:p.Ser101=
NM_018344.6:c.920G= MANE Select	NP_060814.4:p.Ser307=
NM_001174098.2:c.*149G=	NP_001167569.1:n.*149G=
NM_001363518.2:c.686G=	NP_001350447.1:p.Ser229=
NR_033413.2:n.888G=
NR_033414.2:n.661G=