Canonical Allele Identifier: CA209388155

Gene: SLC29A3

Linked Data

• dbSNP Id: rs936901488
• gnomAD v3: 10-71362439-C-T
• gnomAD v4: 10-71362439-C-T
• MyVariant Identifiers: chr10:g.73122196C>T (hg19) ; chr10:g.71362439C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362439C>T , CM000672.2:g.71362439C>T	GRCh38
NC_000010.10:g.73122196C>T , CM000672.1:g.73122196C>T	GRCh37
NC_000010.9:g.72792202C>T	NCBI36
NG_017066.1:g.48187C>T
NG_017066.2:g.48181C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2735C>T
ENST00000373189.6:c.1259C>T MANE Select	ENSP00000362285.5:p.Ser420Phe
ENST00000479577.2:c.1025C>T	ENSP00000493995.1:p.Ser342Phe
ENST00000642198.1:c.*831C>T	ENSP00000494827.1:n.*831C>T
ENST00000642772.1:c.*94+6196C>T	ENSP00000495041.1:n.*94+6196C>T
ENST00000643042.1:c.880C>T	ENSP00000496674.1:n.880C>T
ENST00000643619.1:c.*842C>T	ENSP00000494378.1:n.*842C>T
ENST00000643752.1:c.*585C>T	ENSP00000495000.1:n.*585C>T
ENST00000644088.1:c.*580C>T	ENSP00000494066.1:n.*580C>T
ENST00000644591.1:c.*585C>T	ENSP00000496664.1:n.*585C>T
ENST00000644895.1:c.*99+6196C>T	ENSP00000493872.1:n.*99+6196C>T
ENST00000645345.1:c.*831C>T	ENSP00000495859.1:n.*831C>T
ENST00000647524.1:c.*842C>T	ENSP00000495077.1:n.*842C>T
ENST00000373189.5:c.1259C>T	ENSP00000362285.5:p.Ser420Phe
ENST00000469204.1:n.756C>T
NM_001174098.1:c.*488C>T	NP_001167569.1:n.*488C>T
NM_018344.5:c.1259C>T	NP_060814.4:p.Ser420Phe
NR_033413.1:n.1233C>T
NR_033414.1:n.1006C>T
XM_006717910.2:c.1025C>T	XP_006717973.1:p.Ser342Phe
NM_001363518.1:c.1025C>T	NP_001350447.1:p.Ser342Phe
XM_017016377.2:c.821C>T	XP_016871866.1:p.Ser274Phe
XM_017016378.2:c.641C>T	XP_016871867.1:p.Ser214Phe
NM_018344.6:c.1259C>T MANE Select	NP_060814.4:p.Ser420Phe
NM_001174098.2:c.*488C>T	NP_001167569.1:n.*488C>T
NM_001363518.2:c.1025C>T	NP_001350447.1:p.Ser342Phe
NR_033413.2:n.1227C>T
NR_033414.2:n.1000C>T