Canonical Allele Identifier: CA10068766
Gene: SLC19A1 HGNC NCBI

Linked Data

dbSNP Id: rs1569015847

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45537970_45538040del , CM000683.2:g.45537970_45538040del GRCh38
NC_000021.8:g.46957884_46957954del , CM000683.1:g.46957884_46957954del GRCh37
NC_000021.7:g.45782312_45782382del NCBI36
NG_028278.1:g.9434_9504del
NG_028278.2:g.30106_30176del

Transcript Alleles

HGVS Amino-acid change
ENST00000311124.9:c.-49-30_-9del
ENST00000650808.1:c.-49-30_-9del
ENST00000311124.8:c.-49-30_-9del
ENST00000380010.8:c.-49-30_-9del
ENST00000427839.5:c.-49-30_-9del
ENST00000443742.1:c.-49-30_-9del
ENST00000528477.1:c.-49-30_-9del
ENST00000567670.5:c.-49-30_-9del
NM_001205206.1:c.-49-30_-9del
NM_194255.2:c.-49-30_-9del
XM_005261164.2:c.-407-30_-367del
XM_011529696.1:c.243-30_283del
XM_011529697.1:c.243-30_283del
XM_011529698.1:c.18-30_58del
XM_011529700.1:c.-49-30_-9del
XM_011529701.1:c.-49-30_-9del
XM_011529702.1:c.-49-30_-9del
XM_011529703.1:c.-49-30_-9del
XM_011529704.1:c.-49-30_-9del
XM_011529705.1:c.243-30_283del
XM_011529707.1:c.243-30_283del
XM_011529708.1:c.-49-30_-9del
XM_011529709.1:c.-407-30_-367del
XM_011529710.1:c.-165-5890_-165-5820del XP_011528012.1:n.-165-5890_-165-5820del
NM_001205206.2:c.-49-30_-9del
NM_001352510.1:c.-407-30_-367del
NM_001352511.1:c.-49-30_-9del
NM_001352512.1:c.-49-30_-9del
NM_194255.3:c.-49-30_-9del
XM_011529696.2:c.243-30_283del
XM_011529698.2:c.18-30_58del
XM_011529700.2:c.-49-30_-9del
XM_011529701.2:c.-49-30_-9del
XM_011529702.2:c.-49-30_-9del
XM_011529703.2:c.-49-30_-9del
XM_011529709.2:c.-407-30_-367del
XM_017028443.1:c.156-30_196del
XM_017028444.1:c.243-30_283del
XM_017028445.2:c.243-30_283del
NM_194255.4:c.-49-30_-9del
NM_001205206.3:c.-49-30_-9del
NM_001352510.2:c.-407-30_-367del
NM_001352511.2:c.-49-30_-9del
NM_001352512.2:c.-49-30_-9del
NM_001205206.4:c.-49-30_-9del
NM_001352511.3:c.-49-30_-9del