Canonical Allele Identifier: CA377129563

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73103985T>C (hg19) ; chr10:g.71344228T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71344228T>C , CM000672.2:g.71344228T>C	GRCh38
NC_000010.10:g.73103985T>C , CM000672.1:g.73103985T>C	GRCh37
NC_000010.9:g.72773991T>C	NCBI36
NG_017066.1:g.29976T>C
NG_017066.2:g.29970T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.766T>C
ENST00000373189.6:c.320T>C MANE Select	ENSP00000362285.5:p.Leu107Pro
ENST00000479577.2:c.86T>C	ENSP00000493995.1:p.Leu29Pro
ENST00000642198.1:c.67-7334T>C	ENSP00000494827.1:n.67-7334T>C
ENST00000642772.1:c.301-11853T>C	ENSP00000495041.1:n.301-11853T>C
ENST00000643042.1:c.232-11853T>C	ENSP00000496674.1:n.232-11853T>C
ENST00000643619.1:c.86T>C	ENSP00000494378.1:p.Leu29Pro
ENST00000643752.1:c.320T>C	ENSP00000495000.1:p.Leu107Pro
ENST00000644088.1:c.301-11853T>C	ENSP00000494066.1:n.301-11853T>C
ENST00000644591.1:c.301-7334T>C	ENSP00000496664.1:n.301-7334T>C
ENST00000644895.1:c.301-7334T>C	ENSP00000493872.1:n.301-7334T>C
ENST00000645345.1:c.301-7334T>C	ENSP00000495859.1:n.301-7334T>C
ENST00000647524.1:c.320T>C	ENSP00000495077.1:p.Leu107Pro
ENST00000373189.5:c.320T>C	ENSP00000362285.5:p.Leu107Pro
NM_001174098.1:c.320T>C	NP_001167569.1:p.Leu107Pro
NM_018344.5:c.320T>C	NP_060814.4:p.Leu107Pro
NR_033413.1:n.358-7334T>C
NR_033414.1:n.358-11853T>C
XM_006717910.2:c.86T>C	XP_006717973.1:p.Leu29Pro
XR_946051.1:n.626-2847A>G
NM_001363518.1:c.86T>C	NP_001350447.1:p.Leu29Pro
XM_017016377.2:c.-55-7334T>C	XP_016871866.1:n.-55-7334T>C
XM_017016378.2:c.-8-11853T>C	XP_016871867.1:n.-8-11853T>C
XR_001747496.1:n.1552-2847A>G
XR_001747497.1:n.16A>G
XR_946051.2:n.1552-2847A>G
NM_018344.6:c.320T>C MANE Select	NP_060814.4:p.Leu107Pro
NM_001174098.2:c.320T>C	NP_001167569.1:p.Leu107Pro
NM_001363518.2:c.86T>C	NP_001350447.1:p.Leu29Pro
NR_033413.2:n.352-7334T>C
NR_033414.2:n.352-11853T>C