Canonical Allele Identifier: CA377114267

Gene: SLC29A3

Linked Data

• dbSNP Id: rs1847069311
• gnomAD v3: 10-71362039-G-T
• gnomAD v4: 10-71362039-G-T
• MyVariant Identifiers: chr10:g.73121796G>T (hg19) ; chr10:g.71362039G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362039G>T , CM000672.2:g.71362039G>T	GRCh38
NC_000010.10:g.73121796G>T , CM000672.1:g.73121796G>T	GRCh37
NC_000010.9:g.72791802G>T	NCBI36
NG_017066.1:g.47787G>T
NG_017066.2:g.47781G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2335G>T
ENST00000373189.6:c.859G>T MANE Select	ENSP00000362285.5:p.Ala287Ser
ENST00000479577.2:c.625G>T	ENSP00000493995.1:p.Ala209Ser
ENST00000642198.1:c.*431G>T	ENSP00000494827.1:n.*431G>T
ENST00000642772.1:c.*94+5796G>T	ENSP00000495041.1:n.*94+5796G>T
ENST00000643042.1:c.480G>T	ENSP00000496674.1:n.480G>T
ENST00000643619.1:c.*442G>T	ENSP00000494378.1:n.*442G>T
ENST00000643752.1:c.*185G>T	ENSP00000495000.1:n.*185G>T
ENST00000644088.1:c.*180G>T	ENSP00000494066.1:n.*180G>T
ENST00000644591.1:c.*185G>T	ENSP00000496664.1:n.*185G>T
ENST00000644895.1:c.*99+5796G>T	ENSP00000493872.1:n.*99+5796G>T
ENST00000645345.1:c.*431G>T	ENSP00000495859.1:n.*431G>T
ENST00000647524.1:c.*442G>T	ENSP00000495077.1:n.*442G>T
ENST00000373189.5:c.859G>T	ENSP00000362285.5:p.Ala287Ser
ENST00000469204.1:n.356G>T
NM_001174098.1:c.*88G>T	NP_001167569.1:n.*88G>T
NM_018344.5:c.859G>T	NP_060814.4:p.Ala287Ser
NR_033413.1:n.833G>T
NR_033414.1:n.606G>T
XM_006717910.2:c.625G>T	XP_006717973.1:p.Ala209Ser
NM_001363518.1:c.625G>T	NP_001350447.1:p.Ala209Ser
XM_017016377.2:c.421G>T	XP_016871866.1:p.Ala141Ser
XM_017016378.2:c.241G>T	XP_016871867.1:p.Ala81Ser
NM_018344.6:c.859G>T MANE Select	NP_060814.4:p.Ala287Ser
NM_001174098.2:c.*88G>T	NP_001167569.1:n.*88G>T
NM_001363518.2:c.625G>T	NP_001350447.1:p.Ala209Ser
NR_033413.2:n.827G>T
NR_033414.2:n.600G>T