Canonical Allele Identifier: CA1676974819
Gene: SLC22A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160249146_160249150delinsTAAGG , CM000668.2:g.160249146_160249150delinsTAAGG GRCh38
NC_000006.11:g.160670178_160670182delinsTAAGG , CM000668.1:g.160670178_160670182delinsTAAGG GRCh37
NC_000006.10:g.160590168_160590172delinsTAAGG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366953.8:c.842+66_842+70delinsCCTTA MANE Select ENSP00000355920.3:n.842+66_842+70delinsCC...
ENST00000366952.1:c.779+66_779+70delinsCCTTA ENSP00000355919.1:n.779+66_779+70delinsCC...
ENST00000366953.7:c.842+66_842+70delinsCCTTA ENSP00000355920.3:n.842+66_842+70delinsCC...
ENST00000491092.1:n.739+66_739+70delinsCCTTA
NM_003058.3:c.842+66_842+70delinsCCTTA NP_003049.2:n.842+66_842+70delinsCCTTA
NM_003058.4:c.842+66_842+70delinsCCTTA MANE Select NP_003049.2:n.842+66_842+70delinsCCTTA