Canonical Allele Identifier: CA1206117299

Gene: SLC19A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169485564_169485565delinsTC , CM000663.2:g.169485564_169485565delinsTC	GRCh38
NC_000001.10:g.169454802_169454803delinsTC , CM000663.1:g.169454802_169454803delinsTC	GRCh37
NC_000001.9:g.167721426_167721427delinsTC	NCBI36
NG_008255.1:g.5406_5407delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236137.10:c.202_203delinsGA MANE Select	ENSP00000236137.5:p.Glu68=
ENST00000646596.1:c.202_203delinsGA	ENSP00000494404.1:p.Glu68=
ENST00000236137.9:c.202_203delinsGA	ENSP00000236137.5:p.Glu68=
ENST00000367804.4:c.202_203delinsGA	ENSP00000356778.3:p.Glu68=
NM_006996.2:c.202_203delinsGA	NP_008927.1:p.Glu68=
XM_011509076.1:c.12+488_12+489delinsGA	XP_011507378.1:n.12+488_12+489delinsGA
XM_011509077.1:c.202_203delinsGA	XP_011507379.1:p.Glu68=
NM_001319667.1:c.202_203delinsGA	NP_001306596.1:p.Glu68=
NM_006996.3:c.202_203delinsGA MANE Select	NP_008927.1:p.Glu68=