Canonical Allele Identifier: CA2392215033

Gene: SLC19A1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45546221G= , CM000683.2:g.45546221G=	GRCh38
NC_000021.8:g.46966135G= , CM000683.1:g.46966135G=	GRCh37
NC_000021.7:g.45790563G=	NCBI36
NG_028278.1:g.1251C=
NG_028278.2:g.21923C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000650808.1:c.-49-8213C=	ENSP00000498221.1:n.-49-8213C=
XM_011529697.1:c.-125-1596C=	XP_011527999.1:n.-125-1596C=
XM_011529700.1:c.-49-8213C=	XP_011528002.1:n.-49-8213C=
XM_011529705.1:c.-137-1584C=	XP_011528007.1:n.-137-1584C=
XM_011529707.1:c.-137-1584C=	XP_011528009.1:n.-137-1584C=
XM_011529709.1:c.-407-8213C=	XP_011528011.1:n.-407-8213C=
XM_011529710.1:c.-165-14073C=	XP_011528012.1:n.-165-14073C=
NM_001352511.1:c.-49-8213C=	NP_001339440.1:n.-49-8213C=
XM_011529700.2:c.-49-8213C=	XP_011528002.1:n.-49-8213C=
XM_011529709.2:c.-407-8213C=	XP_011528011.1:n.-407-8213C=
NM_001352511.2:c.-49-8213C=	NP_001339440.1:n.-49-8213C=
NM_001352511.3:c.-49-8213C=	NP_001339440.1:n.-49-8213C=