Canonical Allele Identifier: CA2681064998

Gene: SLC22A1

Linked Data

• gnomAD v4: 6-160139584-C-CATTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160139584_160139585insATTTTTTTTT , CM000668.2:g.160139584_160139585insATTTTTTTTT	GRCh38
NC_000006.11:g.160560616_160560617insATTTTTTTTT , CM000668.1:g.160560616_160560617insATTTTTTTTT	GRCh37
NC_000006.10:g.160480606_160480607insATTTTTTTTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366963.9:c.1062-69_1062-68insATTTTTTTTT MANE Select	ENSP00000355930.4:n.1062-69_1062-68insATTTTTTTTT
ENST00000324965.8:c.1062-69_1062-68insATTTTTTTTT	ENSP00000318103.4:n.1062-69_1062-68insATTTTTTTTT
ENST00000366963.8:c.1062-69_1062-68insATTTTTTTTT	ENSP00000355930.4:n.1062-69_1062-68insATTTTTTTTT
ENST00000457470.6:c.1062-69_1062-68insATTTTTTTTT	ENSP00000409557.2:n.1062-69_1062-68insATTTTTTTTT
ENST00000460902.2:c.1061+2934_1061+2935insATTTTTTTTT	ENSP00000439274.1:n.1061+2934_1061+2935insATTTTTTTTT
ENST00000539263.5:c.*535-69_*535-68insATTTTTTTTT	ENSP00000443245.1:n.*535-69_*535-68insATTTTTTTTT
NM_003057.2:c.1062-69_1062-68insATTTTTTTTT	NP_003048.1:n.1062-69_1062-68insATTTTTTTTT
NM_153187.1:c.1062-69_1062-68insATTTTTTTTT	NP_694857.1:n.1062-69_1062-68insATTTTTTTTT
XM_005267102.3:c.1062-69_1062-68insATTTTTTTTT	XP_005267159.1:n.1062-69_1062-68insATTTTTTTTT
XM_005267103.1:c.1062-69_1062-68insATTTTTTTTT	XP_005267160.1:n.1062-69_1062-68insATTTTTTTTT
XM_005267104.3:c.486-69_486-68insATTTTTTTTT	XP_005267161.1:n.486-69_486-68insATTTTTTTTT
XM_005267105.3:c.486-69_486-68insATTTTTTTTT	XP_005267162.1:n.486-69_486-68insATTTTTTTTT
XM_006715552.1:c.1062-69_1062-68insATTTTTTTTT	XP_006715615.1:n.1062-69_1062-68insATTTTTTTTT
XM_011536074.1:c.486-69_486-68insATTTTTTTTT	XP_011534376.1:n.486-69_486-68insATTTTTTTTT
XM_005267102.5:c.1062-69_1062-68insATTTTTTTTT	XP_005267159.1:n.1062-69_1062-68insATTTTTTTTT
XM_005267103.2:c.1062-69_1062-68insATTTTTTTTT	XP_005267160.1:n.1062-69_1062-68insATTTTTTTTT
XM_005267104.5:c.486-69_486-68insATTTTTTTTT	XP_005267161.1:n.486-69_486-68insATTTTTTTTT
XM_005267105.5:c.486-69_486-68insATTTTTTTTT	XP_005267162.1:n.486-69_486-68insATTTTTTTTT
XM_006715552.2:c.1062-69_1062-68insATTTTTTTTT	XP_006715615.1:n.1062-69_1062-68insATTTTTTTTT
XM_011536074.3:c.486-69_486-68insATTTTTTTTT	XP_011534376.1:n.486-69_486-68insATTTTTTTTT
NM_003057.3:c.1062-69_1062-68insATTTTTTTTT MANE Select	NP_003048.1:n.1062-69_1062-68insATTTTTTTTT
NM_153187.2:c.1062-69_1062-68insATTTTTTTTT	NP_694857.1:n.1062-69_1062-68insATTTTTTTTT