Canonical Allele Identifier: CA1676923701

Gene: SLC22A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160139966_160139975delinsATGAGGTGCT , CM000668.2:g.160139966_160139975delinsATGAGGTGCT	GRCh38
NC_000006.11:g.160560998_160561007delinsATGAGGTGCT , CM000668.1:g.160560998_160561007delinsATGAGGTGCT	GRCh37
NC_000006.10:g.160480988_160480997delinsATGAGGTGCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366963.9:c.1276+99_1276+108delinsATGAGGTGCT MANE Select	ENSP00000355930.4:n.1276+99_1276+108delinsATGAGGTGCT
ENST00000324965.8:c.1276+99_1276+108delinsATGAGGTGCT	ENSP00000318103.4:n.1276+99_1276+108delinsATGAGGTGCT
ENST00000366963.8:c.1276+99_1276+108delinsATGAGGTGCT	ENSP00000355930.4:n.1276+99_1276+108delinsATGAGGTGCT
ENST00000457470.6:c.1276+99_1276+108delinsATGAGGTGCT	ENSP00000409557.2:n.1276+99_1276+108delinsATGAGGTGCT
ENST00000460902.2:c.1061+3316_1061+3325delinsATGAGGTGCT	ENSP00000439274.1:n.1061+3316_1061+3325delinsATGAGGTGCT
ENST00000539263.5:c.*749+99_*749+108delinsATGAGGTGCT	ENSP00000443245.1:n.*749+99_*749+108delinsATGAGGTGCT
NM_003057.2:c.1276+99_1276+108delinsATGAGGTGCT	NP_003048.1:n.1276+99_1276+108delinsATGAGGTGCT
NM_153187.1:c.1276+99_1276+108delinsATGAGGTGCT	NP_694857.1:n.1276+99_1276+108delinsATGAGGTGCT
XM_005267102.3:c.1276+99_1276+108delinsATGAGGTGCT	XP_005267159.1:n.1276+99_1276+108delinsATGAGGTGCT
XM_005267103.1:c.1276+99_1276+108delinsATGAGGTGCT	XP_005267160.1:n.1276+99_1276+108delinsATGAGGTGCT
XM_005267104.3:c.700+99_700+108delinsATGAGGTGCT	XP_005267161.1:n.700+99_700+108delinsATGAGGTGCT
XM_005267105.3:c.700+99_700+108delinsATGAGGTGCT	XP_005267162.1:n.700+99_700+108delinsATGAGGTGCT
XM_006715552.1:c.1276+99_1276+108delinsATGAGGTGCT	XP_006715615.1:n.1276+99_1276+108delinsATGAGGTGCT
XM_011536074.1:c.700+99_700+108delinsATGAGGTGCT	XP_011534376.1:n.700+99_700+108delinsATGAGGTGCT
XM_005267102.5:c.1276+99_1276+108delinsATGAGGTGCT	XP_005267159.1:n.1276+99_1276+108delinsATGAGGTGCT
XM_005267103.2:c.1276+99_1276+108delinsATGAGGTGCT	XP_005267160.1:n.1276+99_1276+108delinsATGAGGTGCT
XM_005267104.5:c.700+99_700+108delinsATGAGGTGCT	XP_005267161.1:n.700+99_700+108delinsATGAGGTGCT
XM_005267105.5:c.700+99_700+108delinsATGAGGTGCT	XP_005267162.1:n.700+99_700+108delinsATGAGGTGCT
XM_006715552.2:c.1276+99_1276+108delinsATGAGGTGCT	XP_006715615.1:n.1276+99_1276+108delinsATGAGGTGCT
XM_011536074.3:c.700+99_700+108delinsATGAGGTGCT	XP_011534376.1:n.700+99_700+108delinsATGAGGTGCT
NM_003057.3:c.1276+99_1276+108delinsATGAGGTGCT MANE Select	NP_003048.1:n.1276+99_1276+108delinsATGAGGTGCT
NM_153187.2:c.1276+99_1276+108delinsATGAGGTGCT	NP_694857.1:n.1276+99_1276+108delinsATGAGGTGCT