Canonical Allele Identifier: CA1956619638
Gene: SLC6A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.20627830_20627831delinsGA , CM000673.2:g.20627830_20627831delinsGA GRCh38
NC_000011.9:g.20649376_20649377delinsGA , CM000673.1:g.20649376_20649377delinsGA GRCh37
NC_000011.8:g.20605952_20605953delinsGA NCBI36
NG_013086.1:g.33431_33432delinsGA
NG_013086.2:g.33431_33432delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000525748.6:c.1396-150_1396-149delinsGA MANE Select ENSP00000434364.2:n.1396-150_1396-149delinsGA
ENST00000298923.11:c.*693-150_*693-149delinsGA ENSP00000298923.7:n.*693-150_*693-149delinsGA
ENST00000525748.5:c.1396-150_1396-149delinsGA ENSP00000434364.1:n.1396-150_1396-149delinsGA
NM_004211.3:c.1396-150_1396-149delinsGA NP_004202.2:n.1396-150_1396-149delinsGA
XM_005253225.1:c.694-150_694-149delinsGA XP_005253282.1:n.694-150_694-149delinsGA
XM_011520473.1:c.1396-150_1396-149delinsGA XP_011518775.1:n.1396-150_1396-149delinsGA
NM_001318369.1:c.694-150_694-149delinsGA NP_001305298.1:n.694-150_694-149delinsGA
NM_004211.4:c.1396-150_1396-149delinsGA NP_004202.3:n.1396-150_1396-149delinsGA
XM_017018544.2:c.520-150_520-149delinsGA XP_016874033.1:n.520-150_520-149delinsGA
XM_017018545.2:c.355-150_355-149delinsGA XP_016874034.1:n.355-150_355-149delinsGA
NM_001318369.2:c.694-150_694-149delinsGA NP_001305298.1:n.694-150_694-149delinsGA
NM_004211.5:c.1396-150_1396-149delinsGA MANE Select NP_004202.4:n.1396-150_1396-149delinsGA