Canonical Allele Identifier: CA1206116128

Gene: SLC19A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169485413_169485416delinsAAAG , CM000663.2:g.169485413_169485416delinsAAAG	GRCh38
NC_000001.10:g.169454651_169454654delinsAAAG , CM000663.1:g.169454651_169454654delinsAAAG	GRCh37
NC_000001.9:g.167721275_167721278delinsAAAG	NCBI36
NG_008255.1:g.5555_5558delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236137.10:c.204+147_204+150delinsCTTT MANE Select	ENSP00000236137.5:n.204+147_204+150delinsCTTT
ENST00000646596.1:c.204+147_204+150delinsCTTT	ENSP00000494404.1:n.204+147_204+150delinsCTTT
ENST00000236137.9:c.204+147_204+150delinsCTTT	ENSP00000236137.5:n.204+147_204+150delinsCTTT
ENST00000367804.4:c.204+147_204+150delinsCTTT	ENSP00000356778.3:n.204+147_204+150delinsCTTT
NM_006996.2:c.204+147_204+150delinsCTTT	NP_008927.1:n.204+147_204+150delinsCTTT
XM_011509076.1:c.12+637_12+640delinsCTTT	XP_011507378.1:n.12+637_12+640delinsCTTT
XM_011509077.1:c.204+147_204+150delinsCTTT	XP_011507379.1:n.204+147_204+150delinsCTTT
NM_001319667.1:c.204+147_204+150delinsCTTT	NP_001306596.1:n.204+147_204+150delinsCTTT
NM_006996.3:c.204+147_204+150delinsCTTT MANE Select	NP_008927.1:n.204+147_204+150delinsCTTT