Canonical Allele Identifier: CA2654931758

Gene: SLC19A1

Linked Data

• gnomAD v4: 21-45544472-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45544472C>A , CM000683.2:g.45544472C>A	GRCh38
NC_000021.8:g.46964386C>A , CM000683.1:g.46964386C>A	GRCh37
NC_000021.7:g.45788814C>A	NCBI36
NG_028278.1:g.3000G>T
NG_028278.2:g.23672G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000650808.1:c.-49-6464G>T	ENSP00000498221.1:n.-49-6464G>T
XM_011529696.1:c.29G>T	XP_011527998.1:p.Arg10Leu
XM_011529697.1:c.29G>T	XP_011527999.1:p.Arg10Leu
XM_011529700.1:c.-49-6464G>T	XP_011528002.1:n.-49-6464G>T
XM_011529705.1:c.29G>T	XP_011528007.1:p.Arg10Leu
XM_011529707.1:c.29G>T	XP_011528009.1:p.Arg10Leu
XM_011529708.1:c.-258G>T	XP_011528010.1:n.-258G>T
XM_011529709.1:c.-407-6464G>T	XP_011528011.1:n.-407-6464G>T
XM_011529710.1:c.-165-12324G>T	XP_011528012.1:n.-165-12324G>T
NM_001352511.1:c.-49-6464G>T	NP_001339440.1:n.-49-6464G>T
XM_011529696.2:c.29G>T	XP_011527998.1:p.Arg10Leu
XM_011529700.2:c.-49-6464G>T	XP_011528002.1:n.-49-6464G>T
XM_011529709.2:c.-407-6464G>T	XP_011528011.1:n.-407-6464G>T
XM_017028444.1:c.29G>T	XP_016883933.1:p.Arg10Leu
XM_017028445.2:c.29G>T	XP_016883934.1:p.Arg10Leu
NM_001352511.2:c.-49-6464G>T	NP_001339440.1:n.-49-6464G>T
NM_001352511.3:c.-49-6464G>T	NP_001339440.1:n.-49-6464G>T