Canonical Allele Identifier: CA2681064994

Gene: SLC22A1

Linked Data

• gnomAD v4: 6-160132192-ACCTCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160132195_160132199del , CM000668.2:g.160132195_160132199del	GRCh38
NC_000006.11:g.160553227_160553231del , CM000668.1:g.160553227_160553231del	GRCh37
NC_000006.10:g.160473217_160473221del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366963.9:c.516-37_516-33del MANE Select	ENSP00000355930.4:n.516-37_516-33del
ENST00000324965.8:c.516-37_516-33del	ENSP00000318103.4:n.516-37_516-33del
ENST00000366963.8:c.516-37_516-33del	ENSP00000355930.4:n.516-37_516-33del
ENST00000457470.6:c.516-37_516-33del	ENSP00000409557.2:n.516-37_516-33del
ENST00000460902.2:c.516-37_516-33del	ENSP00000439274.1:n.516-37_516-33del
ENST00000539263.5:c.412-37_412-33del	ENSP00000443245.1:n.412-37_412-33del
ENST00000540443.1:c.-61-37_-61-33del	ENSP00000440105.1:n.-61-37_-61-33del
NM_003057.2:c.516-37_516-33del	NP_003048.1:n.516-37_516-33del
NM_153187.1:c.516-37_516-33del	NP_694857.1:n.516-37_516-33del
XM_005267102.3:c.516-37_516-33del	XP_005267159.1:n.516-37_516-33del
XM_005267103.1:c.516-37_516-33del	XP_005267160.1:n.516-37_516-33del
XM_005267104.3:c.-61-37_-61-33del	XP_005267161.1:n.-61-37_-61-33del
XM_005267105.3:c.-61-37_-61-33del	XP_005267162.1:n.-61-37_-61-33del
XM_006715552.1:c.516-37_516-33del	XP_006715615.1:n.516-37_516-33del
XM_011536074.1:c.-61-37_-61-33del	XP_011534376.1:n.-61-37_-61-33del
XM_005267102.5:c.516-37_516-33del	XP_005267159.1:n.516-37_516-33del
XM_005267103.2:c.516-37_516-33del	XP_005267160.1:n.516-37_516-33del
XM_005267104.5:c.-61-37_-61-33del	XP_005267161.1:n.-61-37_-61-33del
XM_005267105.5:c.-61-37_-61-33del	XP_005267162.1:n.-61-37_-61-33del
XM_006715552.2:c.516-37_516-33del	XP_006715615.1:n.516-37_516-33del
XM_011536074.3:c.-61-37_-61-33del	XP_011534376.1:n.-61-37_-61-33del
NM_003057.3:c.516-37_516-33del MANE Select	NP_003048.1:n.516-37_516-33del
NM_153187.2:c.516-37_516-33del	NP_694857.1:n.516-37_516-33del