Canonical Allele Identifier: CA10068757

Gene: SLC19A1

Linked Data

• dbSNP Id: rs752578285
• ExAC: 21:46957817 G / A
• gnomAD v2: 21-46957817-G-A
• gnomAD v4: 21-45537903-G-A
• MyVariant Identifiers: chr21:g.46957817G>A (hg19) ; chr21:g.45537903G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45537903G>A , CM000683.2:g.45537903G>A	GRCh38
NC_000021.8:g.46957817G>A , CM000683.1:g.46957817G>A	GRCh37
NC_000021.7:g.45782245G>A	NCBI36
NG_028278.1:g.9569C>T
NG_028278.2:g.30241C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000311124.9:c.57C>T MANE Select	ENSP00000308895.4:p.Asp19=
ENST00000650808.1:c.57C>T	ENSP00000498221.1:p.Asp19=
ENST00000311124.8:c.57C>T	ENSP00000308895.4:p.Asp19=
ENST00000380010.8:c.57C>T	ENSP00000369347.4:p.Asp19=
ENST00000427839.5:c.57C>T	ENSP00000401850.1:p.Asp19=
ENST00000443742.1:c.57C>T	ENSP00000411345.1:p.Asp19=
ENST00000486303.1:n.31C>T
ENST00000528477.1:c.57C>T	ENSP00000435780.1:p.Asp19=
ENST00000567670.5:c.57C>T	ENSP00000457278.1:p.Asp19=
NM_001205206.1:c.57C>T	NP_001192135.1:p.Asp19=
NM_194255.2:c.57C>T	NP_919231.1:p.Asp19=
XM_005261164.2:c.-302C>T	XP_005261221.1:n.-302C>T
XM_011529696.1:c.348C>T	XP_011527998.1:p.Asp116=
XM_011529697.1:c.348C>T	XP_011527999.1:p.Asp116=
XM_011529698.1:c.123C>T	XP_011528000.1:p.Asp41=
XM_011529700.1:c.57C>T	XP_011528002.1:p.Asp19=
XM_011529701.1:c.57C>T	XP_011528003.1:p.Asp19=
XM_011529702.1:c.57C>T	XP_011528004.1:p.Asp19=
XM_011529703.1:c.57C>T	XP_011528005.1:p.Asp19=
XM_011529704.1:c.57C>T	XP_011528006.1:p.Asp19=
XM_011529705.1:c.348C>T	XP_011528007.1:p.Asp116=
XM_011529707.1:c.348C>T	XP_011528009.1:p.Asp116=
XM_011529708.1:c.57C>T	XP_011528010.1:p.Asp19=
XM_011529709.1:c.-302C>T	XP_011528011.1:n.-302C>T
XM_011529710.1:c.-165-5755C>T	XP_011528012.1:n.-165-5755C>T
NM_001205206.2:c.57C>T	NP_001192135.1:p.Asp19=
NM_001352510.1:c.-302C>T	NP_001339439.1:n.-302C>T
NM_001352511.1:c.57C>T	NP_001339440.1:p.Asp19=
NM_001352512.1:c.57C>T	NP_001339441.1:p.Asp19=
NM_194255.3:c.57C>T	NP_919231.1:p.Asp19=
XM_011529696.2:c.348C>T	XP_011527998.1:p.Asp116=
XM_011529698.2:c.123C>T	XP_011528000.1:p.Asp41=
XM_011529700.2:c.57C>T	XP_011528002.1:p.Asp19=
XM_011529701.2:c.57C>T	XP_011528003.1:p.Asp19=
XM_011529702.2:c.57C>T	XP_011528004.1:p.Asp19=
XM_011529703.2:c.57C>T	XP_011528005.1:p.Asp19=
XM_011529709.2:c.-302C>T	XP_011528011.1:n.-302C>T
XM_017028443.1:c.261C>T	XP_016883932.1:p.Asp87=
XM_017028444.1:c.348C>T	XP_016883933.1:p.Asp116=
XM_017028445.2:c.348C>T	XP_016883934.1:p.Asp116=
NM_194255.4:c.57C>T MANE Select	NP_919231.1:p.Asp19=
NM_001205206.3:c.57C>T	NP_001192135.1:p.Asp19=
NM_001352510.2:c.-302C>T	NP_001339439.1:n.-302C>T
NM_001352511.2:c.57C>T	NP_001339440.1:p.Asp19=
NM_001352512.2:c.57C>T	NP_001339441.1:p.Asp19=
NM_001205206.4:c.57C>T	NP_001192135.1:p.Asp19=
NM_001352511.3:c.57C>T	NP_001339440.1:p.Asp19=