Canonical Allele Identifier: CA2392214157
Gene: SLC19A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45544475A= , CM000683.2:g.45544475A= GRCh38
NC_000021.8:g.46964389A= , CM000683.1:g.46964389A= GRCh37
NC_000021.7:g.45788817A= NCBI36
NG_028278.1:g.2997T=
NG_028278.2:g.23669T=

Transcript Alleles

HGVS Amino-acid change
ENST00000650808.1:c.-49-6467T= ENSP00000498221.1:n.-49-6467T=
XM_011529696.1:c.26T= XP_011527998.1:p.Leu9=
XM_011529697.1:c.26T= XP_011527999.1:p.Leu9=
XM_011529700.1:c.-49-6467T= XP_011528002.1:n.-49-6467T=
XM_011529705.1:c.26T= XP_011528007.1:p.Leu9=
XM_011529707.1:c.26T= XP_011528009.1:p.Leu9=
XM_011529708.1:c.-261T= XP_011528010.1:n.-261T=
XM_011529709.1:c.-407-6467T= XP_011528011.1:n.-407-6467T=
XM_011529710.1:c.-165-12327T= XP_011528012.1:n.-165-12327T=
NM_001352511.1:c.-49-6467T= NP_001339440.1:n.-49-6467T=
XM_011529696.2:c.26T= XP_011527998.1:p.Leu9=
XM_011529700.2:c.-49-6467T= XP_011528002.1:n.-49-6467T=
XM_011529709.2:c.-407-6467T= XP_011528011.1:n.-407-6467T=
XM_017028444.1:c.26T= XP_016883933.1:p.Leu9=
XM_017028445.2:c.26T= XP_016883934.1:p.Leu9=
NM_001352511.2:c.-49-6467T= NP_001339440.1:n.-49-6467T=
NM_001352511.3:c.-49-6467T= NP_001339440.1:n.-49-6467T=