Canonical Allele Identifier: CA377129667

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71344284-G-C
• MyVariant Identifiers: chr10:g.73104041G>C (hg19) ; chr10:g.71344284G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71344284G>C , CM000672.2:g.71344284G>C	GRCh38
NC_000010.10:g.73104041G>C , CM000672.1:g.73104041G>C	GRCh37
NC_000010.9:g.72774047G>C	NCBI36
NG_017066.1:g.30032G>C
NG_017066.2:g.30026G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.822G>C
ENST00000373189.6:c.376G>C MANE Select	ENSP00000362285.5:p.Val126Leu
ENST00000479577.2:c.142G>C	ENSP00000493995.1:p.Val48Leu
ENST00000642198.1:c.67-7278G>C	ENSP00000494827.1:n.67-7278G>C
ENST00000642772.1:c.301-11797G>C	ENSP00000495041.1:n.301-11797G>C
ENST00000643042.1:c.232-11797G>C	ENSP00000496674.1:n.232-11797G>C
ENST00000643619.1:c.142G>C	ENSP00000494378.1:p.Val48Leu
ENST00000643752.1:c.376G>C	ENSP00000495000.1:p.Val126Leu
ENST00000644088.1:c.301-11797G>C	ENSP00000494066.1:n.301-11797G>C
ENST00000644591.1:c.301-7278G>C	ENSP00000496664.1:n.301-7278G>C
ENST00000644895.1:c.301-7278G>C	ENSP00000493872.1:n.301-7278G>C
ENST00000645345.1:c.301-7278G>C	ENSP00000495859.1:n.301-7278G>C
ENST00000647524.1:c.376G>C	ENSP00000495077.1:p.Val126Leu
ENST00000373189.5:c.376G>C	ENSP00000362285.5:p.Val126Leu
NM_001174098.1:c.376G>C	NP_001167569.1:p.Val126Leu
NM_018344.5:c.376G>C	NP_060814.4:p.Val126Leu
NR_033413.1:n.358-7278G>C
NR_033414.1:n.358-11797G>C
XM_006717910.2:c.142G>C	XP_006717973.1:p.Val48Leu
XR_946051.1:n.626-2903C>G
NM_001363518.1:c.142G>C	NP_001350447.1:p.Val48Leu
XM_017016377.2:c.-55-7278G>C	XP_016871866.1:n.-55-7278G>C
XM_017016378.2:c.-8-11797G>C	XP_016871867.1:n.-8-11797G>C
XR_001747496.1:n.1552-2903C>G
XR_946051.2:n.1552-2903C>G
NM_018344.6:c.376G>C MANE Select	NP_060814.4:p.Val126Leu
NM_001174098.2:c.376G>C	NP_001167569.1:p.Val126Leu
NM_001363518.2:c.142G>C	NP_001350447.1:p.Val48Leu
NR_033413.2:n.352-7278G>C
NR_033414.2:n.352-11797G>C