Canonical Allele Identifier: CA377116658

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71362291-G-A
• MyVariant Identifiers: chr10:g.73122048G>A (hg19) ; chr10:g.71362291G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362291G>A , CM000672.2:g.71362291G>A	GRCh38
NC_000010.10:g.73122048G>A , CM000672.1:g.73122048G>A	GRCh37
NC_000010.9:g.72792054G>A	NCBI36
NG_017066.1:g.48039G>A
NG_017066.2:g.48033G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2587G>A
ENST00000373189.6:c.1111G>A MANE Select	ENSP00000362285.5:p.Val371Met
ENST00000479577.2:c.877G>A	ENSP00000493995.1:p.Val293Met
ENST00000642198.1:c.*683G>A	ENSP00000494827.1:n.*683G>A
ENST00000642772.1:c.*94+6048G>A	ENSP00000495041.1:n.*94+6048G>A
ENST00000643042.1:c.732G>A	ENSP00000496674.1:n.732G>A
ENST00000643619.1:c.*694G>A	ENSP00000494378.1:n.*694G>A
ENST00000643752.1:c.*437G>A	ENSP00000495000.1:n.*437G>A
ENST00000644088.1:c.*432G>A	ENSP00000494066.1:n.*432G>A
ENST00000644591.1:c.*437G>A	ENSP00000496664.1:n.*437G>A
ENST00000644895.1:c.*99+6048G>A	ENSP00000493872.1:n.*99+6048G>A
ENST00000645345.1:c.*683G>A	ENSP00000495859.1:n.*683G>A
ENST00000647524.1:c.*694G>A	ENSP00000495077.1:n.*694G>A
ENST00000373189.5:c.1111G>A	ENSP00000362285.5:p.Val371Met
ENST00000469204.1:n.608G>A
NM_001174098.1:c.*340G>A	NP_001167569.1:n.*340G>A
NM_018344.5:c.1111G>A	NP_060814.4:p.Val371Met
NR_033413.1:n.1085G>A
NR_033414.1:n.858G>A
XM_006717910.2:c.877G>A	XP_006717973.1:p.Val293Met
NM_001363518.1:c.877G>A	NP_001350447.1:p.Val293Met
XM_017016377.2:c.673G>A	XP_016871866.1:p.Val225Met
XM_017016378.2:c.493G>A	XP_016871867.1:p.Val165Met
NM_018344.6:c.1111G>A MANE Select	NP_060814.4:p.Val371Met
NM_001174098.2:c.*340G>A	NP_001167569.1:n.*340G>A
NM_001363518.2:c.877G>A	NP_001350447.1:p.Val293Met
NR_033413.2:n.1079G>A
NR_033414.2:n.852G>A