Canonical Allele Identifier: CA2497029170

Gene: SLC22A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160139865_160139873delinsCTGGTAAGT , CM000668.2:g.160139865_160139873delinsCTGGTAAGT	GRCh38
NC_000006.11:g.160560897_160560905delinsCTGGTAAGT , CM000668.1:g.160560897_160560905delinsCTGGTAAGT	GRCh37
NC_000006.10:g.160480887_160480895delinsCTGGTAAGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366963.9:c.1274_1276+6delinsCTGGTAAGT
ENST00000324965.8:c.1274_1276+6delinsCTGGTAAGT
ENST00000366963.8:c.1274_1276+6delinsCTGGTAAGT
ENST00000457470.6:c.1274_1276+6delinsCTGGTAAGT
ENST00000460902.2:c.1061+3215_1061+3223delinsCTGGTAAGT	ENSP00000439274.1:n.1061+3215_1061+3223delinsCTGGTAAGT
ENST00000539263.5:c.*747_*749+6delinsCTGGTAAGT
NM_003057.2:c.1274_1276+6delinsCTGGTAAGT
NM_153187.1:c.1274_1276+6delinsCTGGTAAGT
XM_005267102.3:c.1274_1276+6delinsCTGGTAAGT
XM_005267103.1:c.1274_1276+6delinsCTGGTAAGT
XM_005267104.3:c.698_700+6delinsCTGGTAAGT
XM_005267105.3:c.698_700+6delinsCTGGTAAGT
XM_006715552.1:c.1274_1276+6delinsCTGGTAAGT
XM_011536074.1:c.698_700+6delinsCTGGTAAGT
XM_005267102.5:c.1274_1276+6delinsCTGGTAAGT
XM_005267103.2:c.1274_1276+6delinsCTGGTAAGT
XM_005267104.5:c.698_700+6delinsCTGGTAAGT
XM_005267105.5:c.698_700+6delinsCTGGTAAGT
XM_006715552.2:c.1274_1276+6delinsCTGGTAAGT
XM_011536074.3:c.698_700+6delinsCTGGTAAGT
NM_003057.3:c.1274_1276+6delinsCTGGTAAGT
NM_153187.2:c.1274_1276+6delinsCTGGTAAGT