Canonical Allele Identifier: CA377114388

Gene: SLC29A3

Linked Data

• COSMIC: COSM1348885
• MyVariant Identifiers: chr10:g.73121812A>C (hg19) ; chr10:g.71362055A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362055A>C , CM000672.2:g.71362055A>C	GRCh38
NC_000010.10:g.73121812A>C , CM000672.1:g.73121812A>C	GRCh37
NC_000010.9:g.72791818A>C	NCBI36
NG_017066.1:g.47803A>C
NG_017066.2:g.47797A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2351A>C
ENST00000373189.6:c.875A>C MANE Select	ENSP00000362285.5:p.Asp292Ala
ENST00000479577.2:c.641A>C	ENSP00000493995.1:p.Asp214Ala
ENST00000642198.1:c.*447A>C	ENSP00000494827.1:n.*447A>C
ENST00000642772.1:c.*94+5812A>C	ENSP00000495041.1:n.*94+5812A>C
ENST00000643042.1:c.496A>C	ENSP00000496674.1:n.496A>C
ENST00000643619.1:c.*458A>C	ENSP00000494378.1:n.*458A>C
ENST00000643752.1:c.*201A>C	ENSP00000495000.1:n.*201A>C
ENST00000644088.1:c.*196A>C	ENSP00000494066.1:n.*196A>C
ENST00000644591.1:c.*201A>C	ENSP00000496664.1:n.*201A>C
ENST00000644895.1:c.*99+5812A>C	ENSP00000493872.1:n.*99+5812A>C
ENST00000645345.1:c.*447A>C	ENSP00000495859.1:n.*447A>C
ENST00000647524.1:c.*458A>C	ENSP00000495077.1:n.*458A>C
ENST00000373189.5:c.875A>C	ENSP00000362285.5:p.Asp292Ala
ENST00000469204.1:n.372A>C
NM_001174098.1:c.*104A>C	NP_001167569.1:n.*104A>C
NM_018344.5:c.875A>C	NP_060814.4:p.Asp292Ala
NR_033413.1:n.849A>C
NR_033414.1:n.622A>C
XM_006717910.2:c.641A>C	XP_006717973.1:p.Asp214Ala
NM_001363518.1:c.641A>C	NP_001350447.1:p.Asp214Ala
XM_017016377.2:c.437A>C	XP_016871866.1:p.Asp146Ala
XM_017016378.2:c.257A>C	XP_016871867.1:p.Asp86Ala
NM_018344.6:c.875A>C MANE Select	NP_060814.4:p.Asp292Ala
NM_001174098.2:c.*104A>C	NP_001167569.1:n.*104A>C
NM_001363518.2:c.641A>C	NP_001350447.1:p.Asp214Ala
NR_033413.2:n.843A>C
NR_033414.2:n.616A>C