Canonical Allele Identifier: CA377116722

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122052C>A (hg19) ; chr10:g.71362295C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362295C>A , CM000672.2:g.71362295C>A	GRCh38
NC_000010.10:g.73122052C>A , CM000672.1:g.73122052C>A	GRCh37
NC_000010.9:g.72792058C>A	NCBI36
NG_017066.1:g.48043C>A
NG_017066.2:g.48037C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2591C>A
ENST00000373189.6:c.1115C>A MANE Select	ENSP00000362285.5:p.Pro372Gln
ENST00000479577.2:c.881C>A	ENSP00000493995.1:p.Pro294Gln
ENST00000642198.1:c.*687C>A	ENSP00000494827.1:n.*687C>A
ENST00000642772.1:c.*94+6052C>A	ENSP00000495041.1:n.*94+6052C>A
ENST00000643042.1:c.736C>A	ENSP00000496674.1:n.736C>A
ENST00000643619.1:c.*698C>A	ENSP00000494378.1:n.*698C>A
ENST00000643752.1:c.*441C>A	ENSP00000495000.1:n.*441C>A
ENST00000644088.1:c.*436C>A	ENSP00000494066.1:n.*436C>A
ENST00000644591.1:c.*441C>A	ENSP00000496664.1:n.*441C>A
ENST00000644895.1:c.*99+6052C>A	ENSP00000493872.1:n.*99+6052C>A
ENST00000645345.1:c.*687C>A	ENSP00000495859.1:n.*687C>A
ENST00000647524.1:c.*698C>A	ENSP00000495077.1:n.*698C>A
ENST00000373189.5:c.1115C>A	ENSP00000362285.5:p.Pro372Gln
ENST00000469204.1:n.612C>A
NM_001174098.1:c.*344C>A	NP_001167569.1:n.*344C>A
NM_018344.5:c.1115C>A	NP_060814.4:p.Pro372Gln
NR_033413.1:n.1089C>A
NR_033414.1:n.862C>A
XM_006717910.2:c.881C>A	XP_006717973.1:p.Pro294Gln
NM_001363518.1:c.881C>A	NP_001350447.1:p.Pro294Gln
XM_017016377.2:c.677C>A	XP_016871866.1:p.Pro226Gln
XM_017016378.2:c.497C>A	XP_016871867.1:p.Pro166Gln
NM_018344.6:c.1115C>A MANE Select	NP_060814.4:p.Pro372Gln
NM_001174098.2:c.*344C>A	NP_001167569.1:n.*344C>A
NM_001363518.2:c.881C>A	NP_001350447.1:p.Pro294Gln
NR_033413.2:n.1083C>A
NR_033414.2:n.856C>A