Canonical Allele Identifier: CA377116940

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122091T>C (hg19) ; chr10:g.71362334T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362334T>C , CM000672.2:g.71362334T>C	GRCh38
NC_000010.10:g.73122091T>C , CM000672.1:g.73122091T>C	GRCh37
NC_000010.9:g.72792097T>C	NCBI36
NG_017066.1:g.48082T>C
NG_017066.2:g.48076T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2630T>C
ENST00000373189.6:c.1154T>C MANE Select	ENSP00000362285.5:p.Leu385Pro
ENST00000479577.2:c.920T>C	ENSP00000493995.1:p.Leu307Pro
ENST00000642198.1:c.*726T>C	ENSP00000494827.1:n.*726T>C
ENST00000642772.1:c.*94+6091T>C	ENSP00000495041.1:n.*94+6091T>C
ENST00000643042.1:c.775T>C	ENSP00000496674.1:n.775T>C
ENST00000643619.1:c.*737T>C	ENSP00000494378.1:n.*737T>C
ENST00000643752.1:c.*480T>C	ENSP00000495000.1:n.*480T>C
ENST00000644088.1:c.*475T>C	ENSP00000494066.1:n.*475T>C
ENST00000644591.1:c.*480T>C	ENSP00000496664.1:n.*480T>C
ENST00000644895.1:c.*99+6091T>C	ENSP00000493872.1:n.*99+6091T>C
ENST00000645345.1:c.*726T>C	ENSP00000495859.1:n.*726T>C
ENST00000647524.1:c.*737T>C	ENSP00000495077.1:n.*737T>C
ENST00000373189.5:c.1154T>C	ENSP00000362285.5:p.Leu385Pro
ENST00000469204.1:n.651T>C
NM_001174098.1:c.*383T>C	NP_001167569.1:n.*383T>C
NM_018344.5:c.1154T>C	NP_060814.4:p.Leu385Pro
NR_033413.1:n.1128T>C
NR_033414.1:n.901T>C
XM_006717910.2:c.920T>C	XP_006717973.1:p.Leu307Pro
NM_001363518.1:c.920T>C	NP_001350447.1:p.Leu307Pro
XM_017016377.2:c.716T>C	XP_016871866.1:p.Leu239Pro
XM_017016378.2:c.536T>C	XP_016871867.1:p.Leu179Pro
NM_018344.6:c.1154T>C MANE Select	NP_060814.4:p.Leu385Pro
NM_001174098.2:c.*383T>C	NP_001167569.1:n.*383T>C
NM_001363518.2:c.920T>C	NP_001350447.1:p.Leu307Pro
NR_033413.2:n.1122T>C
NR_033414.2:n.895T>C