Canonical Allele Identifier: CA2392214903
Gene: SLC19A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45545981T= , CM000683.2:g.45545981T= GRCh38
NC_000021.8:g.46965895T= , CM000683.1:g.46965895T= GRCh37
NC_000021.7:g.45790323T= NCBI36
NG_028278.1:g.1491A=
NG_028278.2:g.22163A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650808.1:c.-49-7973A= ENSP00000498221.1:n.-49-7973A=
XM_011529697.1:c.-125-1356A= XP_011527999.1:n.-125-1356A=
XM_011529700.1:c.-49-7973A= XP_011528002.1:n.-49-7973A=
XM_011529705.1:c.-137-1344A= XP_011528007.1:n.-137-1344A=
XM_011529707.1:c.-137-1344A= XP_011528009.1:n.-137-1344A=
XM_011529709.1:c.-407-7973A= XP_011528011.1:n.-407-7973A=
XM_011529710.1:c.-165-13833A= XP_011528012.1:n.-165-13833A=
NM_001352511.1:c.-49-7973A= NP_001339440.1:n.-49-7973A=
XM_011529700.2:c.-49-7973A= XP_011528002.1:n.-49-7973A=
XM_011529709.2:c.-407-7973A= XP_011528011.1:n.-407-7973A=
NM_001352511.2:c.-49-7973A= NP_001339440.1:n.-49-7973A=
NM_001352511.3:c.-49-7973A= NP_001339440.1:n.-49-7973A=