Canonical Allele Identifier: CA377114264

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121796G>C (hg19) ; chr10:g.71362039G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2335G>C
ENST00000373189.6:c.859G>C MANE Select	ENSP00000362285.5:p.Ala287Pro
ENST00000479577.2:c.625G>C	ENSP00000493995.1:p.Ala209Pro
ENST00000642198.1:c.*431G>C	ENSP00000494827.1:n.*431G>C
ENST00000642772.1:c.*94+5796G>C	ENSP00000495041.1:n.*94+5796G>C
ENST00000643042.1:c.480G>C	ENSP00000496674.1:n.480G>C
ENST00000643619.1:c.*442G>C	ENSP00000494378.1:n.*442G>C
ENST00000643752.1:c.*185G>C	ENSP00000495000.1:n.*185G>C
ENST00000644088.1:c.*180G>C	ENSP00000494066.1:n.*180G>C
ENST00000644591.1:c.*185G>C	ENSP00000496664.1:n.*185G>C
ENST00000644895.1:c.*99+5796G>C	ENSP00000493872.1:n.*99+5796G>C
ENST00000645345.1:c.*431G>C	ENSP00000495859.1:n.*431G>C
ENST00000647524.1:c.*442G>C	ENSP00000495077.1:n.*442G>C
ENST00000373189.5:c.859G>C	ENSP00000362285.5:p.Ala287Pro
ENST00000469204.1:n.356G>C
NM_001174098.1:c.*88G>C	NP_001167569.1:n.*88G>C
NM_018344.5:c.859G>C	NP_060814.4:p.Ala287Pro
NR_033413.1:n.833G>C
NR_033414.1:n.606G>C
XM_006717910.2:c.625G>C	XP_006717973.1:p.Ala209Pro
NM_001363518.1:c.625G>C	NP_001350447.1:p.Ala209Pro
XM_017016377.2:c.421G>C	XP_016871866.1:p.Ala141Pro
XM_017016378.2:c.241G>C	XP_016871867.1:p.Ala81Pro
NM_018344.6:c.859G>C MANE Select	NP_060814.4:p.Ala287Pro
NM_001174098.2:c.*88G>C	NP_001167569.1:n.*88G>C
NM_001363518.2:c.625G>C	NP_001350447.1:p.Ala209Pro
NR_033413.2:n.827G>C
NR_033414.2:n.600G>C