Canonical Allele Identifier: CA2392214126
Gene: SLC19A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45544401C= , CM000683.2:g.45544401C= GRCh38
NC_000021.8:g.46964315C= , CM000683.1:g.46964315C= GRCh37
NC_000021.7:g.45788743C= NCBI36
NG_028278.1:g.3071G=
NG_028278.2:g.23743G=

Transcript Alleles

HGVS Amino-acid change
ENST00000650808.1:c.-49-6393G= ENSP00000498221.1:n.-49-6393G=
ENST00000528477.1:c.-397G= ENSP00000435780.1:n.-397G=
ENST00000567670.5:c.-314G= ENSP00000457278.1:n.-314G=
XM_011529696.1:c.33-55G= XP_011527998.1:n.33-55G=
XM_011529697.1:c.33-55G= XP_011527999.1:n.33-55G=
XM_011529700.1:c.-49-6393G= XP_011528002.1:n.-49-6393G=
XM_011529701.1:c.-397G= XP_011528003.1:n.-397G=
XM_011529705.1:c.33-55G= XP_011528007.1:n.33-55G=
XM_011529707.1:c.33-55G= XP_011528009.1:n.33-55G=
XM_011529708.1:c.-254-60G= XP_011528010.1:n.-254-60G=
XM_011529709.1:c.-407-6393G= XP_011528011.1:n.-407-6393G=
XM_011529710.1:c.-165-12253G= XP_011528012.1:n.-165-12253G=
NM_001352511.1:c.-49-6393G= NP_001339440.1:n.-49-6393G=
XM_011529696.2:c.33-55G= XP_011527998.1:n.33-55G=
XM_011529700.2:c.-49-6393G= XP_011528002.1:n.-49-6393G=
XM_011529701.2:c.-397G= XP_011528003.1:n.-397G=
XM_011529709.2:c.-407-6393G= XP_011528011.1:n.-407-6393G=
XM_017028444.1:c.33-55G= XP_016883933.1:n.33-55G=
XM_017028445.2:c.33-55G= XP_016883934.1:n.33-55G=
NM_001352511.2:c.-49-6393G= NP_001339440.1:n.-49-6393G=
NM_001352511.3:c.-49-6393G= NP_001339440.1:n.-49-6393G=