Canonical Allele Identifier: CA2681065062

Gene: SLC22A1

Linked Data

• gnomAD v4: 6-160139600-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160139600_160139601insC , CM000668.2:g.160139600_160139601insC	GRCh38
NC_000006.11:g.160560632_160560633insC , CM000668.1:g.160560632_160560633insC	GRCh37
NC_000006.10:g.160480622_160480623insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366963.9:c.1062-53_1062-52insC MANE Select	ENSP00000355930.4:n.1062-53_1062-52insC
ENST00000324965.8:c.1062-53_1062-52insC	ENSP00000318103.4:n.1062-53_1062-52insC
ENST00000366963.8:c.1062-53_1062-52insC	ENSP00000355930.4:n.1062-53_1062-52insC
ENST00000457470.6:c.1062-53_1062-52insC	ENSP00000409557.2:n.1062-53_1062-52insC
ENST00000460902.2:c.1061+2950_1061+2951insC	ENSP00000439274.1:n.1061+2950_1061+2951insC
ENST00000539263.5:c.*535-53_*535-52insC	ENSP00000443245.1:n.*535-53_*535-52insC
NM_003057.2:c.1062-53_1062-52insC	NP_003048.1:n.1062-53_1062-52insC
NM_153187.1:c.1062-53_1062-52insC	NP_694857.1:n.1062-53_1062-52insC
XM_005267102.3:c.1062-53_1062-52insC	XP_005267159.1:n.1062-53_1062-52insC
XM_005267103.1:c.1062-53_1062-52insC	XP_005267160.1:n.1062-53_1062-52insC
XM_005267104.3:c.486-53_486-52insC	XP_005267161.1:n.486-53_486-52insC
XM_005267105.3:c.486-53_486-52insC	XP_005267162.1:n.486-53_486-52insC
XM_006715552.1:c.1062-53_1062-52insC	XP_006715615.1:n.1062-53_1062-52insC
XM_011536074.1:c.486-53_486-52insC	XP_011534376.1:n.486-53_486-52insC
XM_005267102.5:c.1062-53_1062-52insC	XP_005267159.1:n.1062-53_1062-52insC
XM_005267103.2:c.1062-53_1062-52insC	XP_005267160.1:n.1062-53_1062-52insC
XM_005267104.5:c.486-53_486-52insC	XP_005267161.1:n.486-53_486-52insC
XM_005267105.5:c.486-53_486-52insC	XP_005267162.1:n.486-53_486-52insC
XM_006715552.2:c.1062-53_1062-52insC	XP_006715615.1:n.1062-53_1062-52insC
XM_011536074.3:c.486-53_486-52insC	XP_011534376.1:n.486-53_486-52insC
NM_003057.3:c.1062-53_1062-52insC MANE Select	NP_003048.1:n.1062-53_1062-52insC
NM_153187.2:c.1062-53_1062-52insC	NP_694857.1:n.1062-53_1062-52insC