Canonical Allele Identifier: CA1676974834
Gene: SLC22A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160249180_160249184delinsTTTGA , CM000668.2:g.160249180_160249184delinsTTTGA GRCh38
NC_000006.11:g.160670212_160670216delinsTTTGA , CM000668.1:g.160670212_160670216delinsTTTGA GRCh37
NC_000006.10:g.160590202_160590206delinsTTTGA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366953.8:c.842+32_842+36delinsTCAAA MANE Select ENSP00000355920.3:n.842+32_842+36delinsTC...
ENST00000366952.1:c.779+32_779+36delinsTCAAA ENSP00000355919.1:n.779+32_779+36delinsTC...
ENST00000366953.7:c.842+32_842+36delinsTCAAA ENSP00000355920.3:n.842+32_842+36delinsTC...
ENST00000491092.1:n.739+32_739+36delinsTCAAA
NM_003058.3:c.842+32_842+36delinsTCAAA NP_003049.2:n.842+32_842+36delinsTCAAA
NM_003058.4:c.842+32_842+36delinsTCAAA MANE Select NP_003049.2:n.842+32_842+36delinsTCAAA