Canonical Allele Identifier: CA377114610

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121842T>C (hg19) ; chr10:g.71362085T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362085T>C , CM000672.2:g.71362085T>C	GRCh38
NC_000010.10:g.73121842T>C , CM000672.1:g.73121842T>C	GRCh37
NC_000010.9:g.72791848T>C	NCBI36
NG_017066.1:g.47833T>C
NG_017066.2:g.47827T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2381T>C
ENST00000373189.6:c.905T>C MANE Select	ENSP00000362285.5:p.Leu302Pro
ENST00000479577.2:c.671T>C	ENSP00000493995.1:p.Leu224Pro
ENST00000642198.1:c.*477T>C	ENSP00000494827.1:n.*477T>C
ENST00000642772.1:c.*94+5842T>C	ENSP00000495041.1:n.*94+5842T>C
ENST00000643042.1:c.526T>C	ENSP00000496674.1:n.526T>C
ENST00000643619.1:c.*488T>C	ENSP00000494378.1:n.*488T>C
ENST00000643752.1:c.*231T>C	ENSP00000495000.1:n.*231T>C
ENST00000644088.1:c.*226T>C	ENSP00000494066.1:n.*226T>C
ENST00000644591.1:c.*231T>C	ENSP00000496664.1:n.*231T>C
ENST00000644895.1:c.*99+5842T>C	ENSP00000493872.1:n.*99+5842T>C
ENST00000645345.1:c.*477T>C	ENSP00000495859.1:n.*477T>C
ENST00000647524.1:c.*488T>C	ENSP00000495077.1:n.*488T>C
ENST00000373189.5:c.905T>C	ENSP00000362285.5:p.Leu302Pro
ENST00000469204.1:n.402T>C
NM_001174098.1:c.*134T>C	NP_001167569.1:n.*134T>C
NM_018344.5:c.905T>C	NP_060814.4:p.Leu302Pro
NR_033413.1:n.879T>C
NR_033414.1:n.652T>C
XM_006717910.2:c.671T>C	XP_006717973.1:p.Leu224Pro
NM_001363518.1:c.671T>C	NP_001350447.1:p.Leu224Pro
XM_017016377.2:c.467T>C	XP_016871866.1:p.Leu156Pro
XM_017016378.2:c.287T>C	XP_016871867.1:p.Leu96Pro
NM_018344.6:c.905T>C MANE Select	NP_060814.4:p.Leu302Pro
NM_001174098.2:c.*134T>C	NP_001167569.1:n.*134T>C
NM_001363518.2:c.671T>C	NP_001350447.1:p.Leu224Pro
NR_033413.2:n.873T>C
NR_033414.2:n.646T>C