Canonical Allele Identifier: CA470280944

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121813T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362056T>C , CM000672.2:g.71362056T>C	GRCh38
NC_000010.10:g.73121813T>C , CM000672.1:g.73121813T>C	GRCh37
NC_000010.9:g.72791819T>C	NCBI36
NG_017066.1:g.47804T>C
NG_017066.2:g.47798T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2352T>C
ENST00000373189.6:c.876T>C MANE Select	ENSP00000362285.5:p.Asp292=
ENST00000479577.2:c.642T>C	ENSP00000493995.1:p.Asp214=
ENST00000642198.1:c.*448T>C	ENSP00000494827.1:n.*448T>C
ENST00000642772.1:c.*94+5813T>C	ENSP00000495041.1:n.*94+5813T>C
ENST00000643042.1:c.497T>C	ENSP00000496674.1:n.497T>C
ENST00000643619.1:c.*459T>C	ENSP00000494378.1:n.*459T>C
ENST00000643752.1:c.*202T>C	ENSP00000495000.1:n.*202T>C
ENST00000644088.1:c.*197T>C	ENSP00000494066.1:n.*197T>C
ENST00000644591.1:c.*202T>C	ENSP00000496664.1:n.*202T>C
ENST00000644895.1:c.*99+5813T>C	ENSP00000493872.1:n.*99+5813T>C
ENST00000645345.1:c.*448T>C	ENSP00000495859.1:n.*448T>C
ENST00000647524.1:c.*459T>C	ENSP00000495077.1:n.*459T>C
ENST00000373189.5:c.876T>C	ENSP00000362285.5:p.Asp292=
ENST00000469204.1:n.373T>C
NM_001174098.1:c.*105T>C	NP_001167569.1:n.*105T>C
NM_018344.5:c.876T>C	NP_060814.4:p.Asp292=
NR_033413.1:n.850T>C
NR_033414.1:n.623T>C
XM_006717910.2:c.642T>C	XP_006717973.1:p.Asp214=
NM_001363518.1:c.642T>C	NP_001350447.1:p.Asp214=
XM_017016377.2:c.438T>C	XP_016871866.1:p.Asp146=
XM_017016378.2:c.258T>C	XP_016871867.1:p.Asp86=
NM_018344.6:c.876T>C MANE Select	NP_060814.4:p.Asp292=
NM_001174098.2:c.*105T>C	NP_001167569.1:n.*105T>C
NM_001363518.2:c.642T>C	NP_001350447.1:p.Asp214=
NR_033413.2:n.844T>C
NR_033414.2:n.617T>C