Canonical Allele Identifier: CA1206116123

Gene: SLC19A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169485396_169485398delinsCAG , CM000663.2:g.169485396_169485398delinsCAG	GRCh38
NC_000001.10:g.169454634_169454636delinsCAG , CM000663.1:g.169454634_169454636delinsCAG	GRCh37
NC_000001.9:g.167721258_167721260delinsCAG	NCBI36
NG_008255.1:g.5573_5575delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236137.10:c.204+165_204+167delinsCTG MANE Select	ENSP00000236137.5:n.204+165_204+167delinsCTG
ENST00000646596.1:c.204+165_204+167delinsCTG	ENSP00000494404.1:n.204+165_204+167delinsCTG
ENST00000236137.9:c.204+165_204+167delinsCTG	ENSP00000236137.5:n.204+165_204+167delinsCTG
ENST00000367804.4:c.204+165_204+167delinsCTG	ENSP00000356778.3:n.204+165_204+167delinsCTG
NM_006996.2:c.204+165_204+167delinsCTG	NP_008927.1:n.204+165_204+167delinsCTG
XM_011509076.1:c.12+655_12+657delinsCTG	XP_011507378.1:n.12+655_12+657delinsCTG
XM_011509077.1:c.204+165_204+167delinsCTG	XP_011507379.1:n.204+165_204+167delinsCTG
NM_001319667.1:c.204+165_204+167delinsCTG	NP_001306596.1:n.204+165_204+167delinsCTG
NM_006996.3:c.204+165_204+167delinsCTG MANE Select	NP_008927.1:n.204+165_204+167delinsCTG