Canonical Allele Identifier: CA1918678454
Gene: SLC29A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71362327G= , CM000672.2:g.71362327G= GRCh38
NC_000010.10:g.73122084G= , CM000672.1:g.73122084G= GRCh37
NC_000010.9:g.72792090G= NCBI36
NG_017066.1:g.48075G=
NG_017066.2:g.48069G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697843.1:n.2623G=
ENST00000373189.6:c.1147G= MANE Select ENSP00000362285.5:p.Val383=
ENST00000479577.2:c.913G= ENSP00000493995.1:p.Val305=
ENST00000642198.1:c.*719G= ENSP00000494827.1:n.*719G=
ENST00000642772.1:c.*94+6084G= ENSP00000495041.1:n.*94+6084G=
ENST00000643042.1:c.768G= ENSP00000496674.1:n.768G=
ENST00000643619.1:c.*730G= ENSP00000494378.1:n.*730G=
ENST00000643752.1:c.*473G= ENSP00000495000.1:n.*473G=
ENST00000644088.1:c.*468G= ENSP00000494066.1:n.*468G=
ENST00000644591.1:c.*473G= ENSP00000496664.1:n.*473G=
ENST00000644895.1:c.*99+6084G= ENSP00000493872.1:n.*99+6084G=
ENST00000645345.1:c.*719G= ENSP00000495859.1:n.*719G=
ENST00000647524.1:c.*730G= ENSP00000495077.1:n.*730G=
ENST00000373189.5:c.1147G= ENSP00000362285.5:p.Val383=
ENST00000469204.1:n.644G=
NM_001174098.1:c.*376G= NP_001167569.1:n.*376G=
NM_018344.5:c.1147G= NP_060814.4:p.Val383=
NR_033413.1:n.1121G=
NR_033414.1:n.894G=
XM_006717910.2:c.913G= XP_006717973.1:p.Val305=
NM_001363518.1:c.913G= NP_001350447.1:p.Val305=
XM_017016377.2:c.709G= XP_016871866.1:p.Val237=
XM_017016378.2:c.529G= XP_016871867.1:p.Val177=
NM_018344.6:c.1147G= MANE Select NP_060814.4:p.Val383=
NM_001174098.2:c.*376G= NP_001167569.1:n.*376G=
NM_001363518.2:c.913G= NP_001350447.1:p.Val305=
NR_033413.2:n.1115G=
NR_033414.2:n.888G=