Canonical Allele Identifier: CA1206116114

Gene: SLC19A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169485387_169485388delinsCG , CM000663.2:g.169485387_169485388delinsCG	GRCh38
NC_000001.10:g.169454625_169454626delinsCG , CM000663.1:g.169454625_169454626delinsCG	GRCh37
NC_000001.9:g.167721249_167721250delinsCG	NCBI36
NG_008255.1:g.5583_5584delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236137.10:c.204+175_204+176delinsCG MANE Select	ENSP00000236137.5:n.204+175_204+176delinsCG
ENST00000646596.1:c.204+175_204+176delinsCG	ENSP00000494404.1:n.204+175_204+176delinsCG
ENST00000236137.9:c.204+175_204+176delinsCG	ENSP00000236137.5:n.204+175_204+176delinsCG
ENST00000367804.4:c.204+175_204+176delinsCG	ENSP00000356778.3:n.204+175_204+176delinsCG
NM_006996.2:c.204+175_204+176delinsCG	NP_008927.1:n.204+175_204+176delinsCG
XM_011509076.1:c.12+665_12+666delinsCG	XP_011507378.1:n.12+665_12+666delinsCG
XM_011509077.1:c.204+175_204+176delinsCG	XP_011507379.1:n.204+175_204+176delinsCG
NM_001319667.1:c.204+175_204+176delinsCG	NP_001306596.1:n.204+175_204+176delinsCG
NM_006996.3:c.204+175_204+176delinsCG MANE Select	NP_008927.1:n.204+175_204+176delinsCG