Canonical Allele Identifier: CA2392210533
Gene: SLC19A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45537907G= , CM000683.2:g.45537907G= GRCh38
NC_000021.8:g.46957821G= , CM000683.1:g.46957821G= GRCh37
NC_000021.7:g.45782249G= NCBI36
NG_028278.1:g.9565C=
NG_028278.2:g.30237C=

Transcript Alleles

HGVS Amino-acid change
ENST00000311124.9:c.53C= MANE Select ENSP00000308895.4:p.Pro18=
ENST00000650808.1:c.53C= ENSP00000498221.1:p.Pro18=
ENST00000311124.8:c.53C= ENSP00000308895.4:p.Pro18=
ENST00000380010.8:c.53C= ENSP00000369347.4:p.Pro18=
ENST00000427839.5:c.53C= ENSP00000401850.1:p.Pro18=
ENST00000443742.1:c.53C= ENSP00000411345.1:p.Pro18=
ENST00000486303.1:n.27C=
ENST00000528477.1:c.53C= ENSP00000435780.1:p.Pro18=
ENST00000567670.5:c.53C= ENSP00000457278.1:p.Pro18=
NM_001205206.1:c.53C= NP_001192135.1:p.Pro18=
NM_194255.2:c.53C= NP_919231.1:p.Pro18=
XM_005261164.2:c.-306C= XP_005261221.1:n.-306C=
XM_011529696.1:c.344C= XP_011527998.1:p.Pro115=
XM_011529697.1:c.344C= XP_011527999.1:p.Pro115=
XM_011529698.1:c.119C= XP_011528000.1:p.Pro40=
XM_011529700.1:c.53C= XP_011528002.1:p.Pro18=
XM_011529701.1:c.53C= XP_011528003.1:p.Pro18=
XM_011529702.1:c.53C= XP_011528004.1:p.Pro18=
XM_011529703.1:c.53C= XP_011528005.1:p.Pro18=
XM_011529704.1:c.53C= XP_011528006.1:p.Pro18=
XM_011529705.1:c.344C= XP_011528007.1:p.Pro115=
XM_011529707.1:c.344C= XP_011528009.1:p.Pro115=
XM_011529708.1:c.53C= XP_011528010.1:p.Pro18=
XM_011529709.1:c.-306C= XP_011528011.1:n.-306C=
XM_011529710.1:c.-165-5759C= XP_011528012.1:n.-165-5759C=
NM_001205206.2:c.53C= NP_001192135.1:p.Pro18=
NM_001352510.1:c.-306C= NP_001339439.1:n.-306C=
NM_001352511.1:c.53C= NP_001339440.1:p.Pro18=
NM_001352512.1:c.53C= NP_001339441.1:p.Pro18=
NM_194255.3:c.53C= NP_919231.1:p.Pro18=
XM_011529696.2:c.344C= XP_011527998.1:p.Pro115=
XM_011529698.2:c.119C= XP_011528000.1:p.Pro40=
XM_011529700.2:c.53C= XP_011528002.1:p.Pro18=
XM_011529701.2:c.53C= XP_011528003.1:p.Pro18=
XM_011529702.2:c.53C= XP_011528004.1:p.Pro18=
XM_011529703.2:c.53C= XP_011528005.1:p.Pro18=
XM_011529709.2:c.-306C= XP_011528011.1:n.-306C=
XM_017028443.1:c.257C= XP_016883932.1:p.Pro86=
XM_017028444.1:c.344C= XP_016883933.1:p.Pro115=
XM_017028445.2:c.344C= XP_016883934.1:p.Pro115=
NM_194255.4:c.53C= MANE Select NP_919231.1:p.Pro18=
NM_001205206.3:c.53C= NP_001192135.1:p.Pro18=
NM_001352510.2:c.-306C= NP_001339439.1:n.-306C=
NM_001352511.2:c.53C= NP_001339440.1:p.Pro18=
NM_001352512.2:c.53C= NP_001339441.1:p.Pro18=
NM_001205206.4:c.53C= NP_001192135.1:p.Pro18=
NM_001352511.3:c.53C= NP_001339440.1:p.Pro18=