Canonical Allele Identifier: CA1206117372

Gene: SLC19A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169485699G= , CM000663.2:g.169485699G=	GRCh38
NC_000001.10:g.169454937G= , CM000663.1:g.169454937G=	GRCh37
NC_000001.9:g.167721561G=	NCBI36
NG_008255.1:g.5272C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236137.10:c.68C= MANE Select	ENSP00000236137.5:p.Ala23=
ENST00000646596.1:c.68C=	ENSP00000494404.1:p.Ala23=
ENST00000236137.9:c.68C=	ENSP00000236137.5:p.Ala23=
ENST00000367804.4:c.68C=	ENSP00000356778.3:p.Ala23=
NM_006996.2:c.68C=	NP_008927.1:p.Ala23=
XM_011509076.1:c.12+354C=	XP_011507378.1:n.12+354C=
XM_011509077.1:c.68C=	XP_011507379.1:p.Ala23=
NM_001319667.1:c.68C=	NP_001306596.1:p.Ala23=
NM_006996.3:c.68C= MANE Select	NP_008927.1:p.Ala23=