Canonical Allele Identifier: CA1140886887

Gene: SLC19A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169468793C= , CM000663.2:g.169468793C=	GRCh38
NC_000001.10:g.169438031C= , CM000663.1:g.169438031C=	GRCh37
NC_000001.9:g.167704655C=	NCBI36
NG_008255.1:g.22178G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236137.10:c.1074G= MANE Select	ENSP00000236137.5:p.Trp358=
ENST00000643377.1:n.405G=
ENST00000646596.1:c.1031-56G=	ENSP00000494404.1:n.1031-56G=
ENST00000236137.9:c.1074G=	ENSP00000236137.5:p.Trp358=
ENST00000367804.4:c.471G=	ENSP00000356778.3:p.Trp157=
NM_006996.2:c.1074G=	NP_008927.1:p.Trp358=
XM_011509076.1:c.882G=	XP_011507378.1:p.Trp294=
XM_011509077.1:c.471G=	XP_011507379.1:p.Trp157=
NM_001319667.1:c.471G=	NP_001306596.1:p.Trp157=
NM_006996.3:c.1074G= MANE Select	NP_008927.1:p.Trp358=