Canonical Allele Identifier: CA470281092

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121870T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362113T>C , CM000672.2:g.71362113T>C	GRCh38
NC_000010.10:g.73121870T>C , CM000672.1:g.73121870T>C	GRCh37
NC_000010.9:g.72791876T>C	NCBI36
NG_017066.1:g.47861T>C
NG_017066.2:g.47855T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2409T>C
ENST00000373189.6:c.933T>C MANE Select	ENSP00000362285.5:p.Cys311=
ENST00000479577.2:c.699T>C	ENSP00000493995.1:p.Cys233=
ENST00000642198.1:c.*505T>C	ENSP00000494827.1:n.*505T>C
ENST00000642772.1:c.*94+5870T>C	ENSP00000495041.1:n.*94+5870T>C
ENST00000643042.1:c.554T>C	ENSP00000496674.1:n.554T>C
ENST00000643619.1:c.*516T>C	ENSP00000494378.1:n.*516T>C
ENST00000643752.1:c.*259T>C	ENSP00000495000.1:n.*259T>C
ENST00000644088.1:c.*254T>C	ENSP00000494066.1:n.*254T>C
ENST00000644591.1:c.*259T>C	ENSP00000496664.1:n.*259T>C
ENST00000644895.1:c.*99+5870T>C	ENSP00000493872.1:n.*99+5870T>C
ENST00000645345.1:c.*505T>C	ENSP00000495859.1:n.*505T>C
ENST00000647524.1:c.*516T>C	ENSP00000495077.1:n.*516T>C
ENST00000373189.5:c.933T>C	ENSP00000362285.5:p.Cys311=
ENST00000469204.1:n.430T>C
NM_001174098.1:c.*162T>C	NP_001167569.1:n.*162T>C
NM_018344.5:c.933T>C	NP_060814.4:p.Cys311=
NR_033413.1:n.907T>C
NR_033414.1:n.680T>C
XM_006717910.2:c.699T>C	XP_006717973.1:p.Cys233=
NM_001363518.1:c.699T>C	NP_001350447.1:p.Cys233=
XM_017016377.2:c.495T>C	XP_016871866.1:p.Cys165=
XM_017016378.2:c.315T>C	XP_016871867.1:p.Cys105=
NM_018344.6:c.933T>C MANE Select	NP_060814.4:p.Cys311=
NM_001174098.2:c.*162T>C	NP_001167569.1:n.*162T>C
NM_001363518.2:c.699T>C	NP_001350447.1:p.Cys233=
NR_033413.2:n.901T>C
NR_033414.2:n.674T>C